Kin-Country Syndrome Post Cold War Era

Kin-Country Syndrome Post Cold War
The kin–country syndrome is the one of the premise by Samuel Huntington that concerning to the
Clash of Civilizations. The kin–country syndrome is the conditions where groups or states are
belonging one civilization. But, they involved to the war with the other people that come from the
different civilization. They have a purpose to rally support from the other members of their own
civilization. The kin–country syndrome are changing the political ideology and the tradition balance
the power deliberation of the standards arguments for cooperation and coalitions. It is emerging
slowly the conflicts in the Post–Cold War circumstances.
There are some elements of rallying the civilizations. This elements are important because of the
continuity
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Sturge-Weber Syndrome Research Paper
Sturge–Weber Syndrome Kris Avila 08/30/2015 NURSPT 030L Mrs. B Abstract According to the
Sturge–Weber Foundations, Sturge–Weber Syndrome can be diagnosed once the baby is born. With
the most obvious characteristics, the baby will have a dark purple birthmark that covers close to half
of his/her face. Another symptom from Sturge–Weber Syndrome is that it can cause neurological
deformity. Both of these symptoms are caused by the abnormal blood vessels near the eye and on
the surface of the brain. Studies have shown that this syndrome is not passed from family history,
but the only remedy we can do is to suppress it (Sturge–Weber.org). One of the most amazing
miracles in life is when a child is born. Upon birth, ... Show more content on Helpwriting.net ...
The only way to cope with the disease is to control it and improving the person's lifestyle. (Moore,
2012). Pinpointing what kind of symptoms and category of Sturge–Weber Syndrome the person has,
an MD can figure out what types of remedies are available. There are many different types of
pharmacologic treatments for seizures. Most of the seizures from the disease are located only on one
side of the brain's hemisphere. Some of the medications include Carbamazepine, Phenytoin,
Oxcarbazepine, Lamotrigine, Levetiracetam, Valproic Acid, Zonisamide, Topiramate, Lorazepam,
Phenobarbital, Gabapentin, Pregabalin, Tiagabine, Diazepam, Felbamate, Lacosamide, and
Clonazepam. With the seizures being controlled with medications, it helped prevent future seizures
from 10% to 50%. Besides medications, there are also surgical treatments available as well. Early
surgery for patients with Sturge–Weber Syndrome is to improve and prevent developmental delay,
refractory seizures, and hemiparesis. Lobectomy and craniotomy were recommended once being
diagnosed with the disease because doctors have found that early onsets of seizures can lead towards
mental retardatation. A procedure called hemispherectomy is also recommended to be given when a
unilateral epileptogenic region exist. This procedure is also done while the patient is still young. It is
preferable because the epileptogenic region is smaller. Studies have shown

Prader Willie Syndrome Research Paper
Disability Research Activity
(Prader–Willie Syndrome)
Disability
Prader–Willie Syndrome a rare congenital disorder characterized by learning difficulties, growth
abnormalities, and obsessive eating, caused especially by the absence of certain genes normally
present on the copy of chromosome 15 inherited from the father.
Characteristics & Effects
Short stature
Small hands and feet
An abnormal body composition (reduced lean tissue and increased fat mass)
Developmental delay
Mild to moderate intellectual disability
Characteristic behaviors and psychological problems
Low levels of growth hormone and sex hormones are common
Thyroid function may be impaired
Floppiness and weak muscles that becomes apparent during or shortly after birth
Feeding problems and failure to grow during ... Show more content on Helpwriting.net ...
Replacement of sex hormones during puberty may result in development of adequate secondary sex
characteristics e.g. breasts, pubic hair and a deeper voice.
How it is diagnosed
Genetic testing can be used to check blood for the genetic abnormalities known to cause PWS.
Any suspected diagnosis of PWS is usually made by a physician based on clinical symptoms.
The preferred method of testing is a "methylation analysis," which detects >99% of cases.
A "FISH" (fluorescent in–situ hybridization) test will identify those patients with PWS due to a
deletion, but it will not identify those who have PWS by "UPD" (uniparental disomy) or an
imprinting error.
PWS can be detected before birth if the mother undergoes amniocentesis testing or chorionic villus
sampling but this testing is only recommended if the mother or father is known to have a
chromosome rearrangement, or if they already have a child with PWS.
Incidence in the population
Approximately one out of every 15,000 births.

Males and females equally effected as are all races and ethnicities.
Most common genetic cause of life–threatening childhood obesity.

Down Syndrome
CHAPTER 1: THE PROBLEM
A. INTRODUCTION
Having a Down syndrome is such a difficult situation for an individual to have. They have slow
physical and mental capabilities that lead them to discrimination. Physical features of having a
Down syndrome. Including flattening of the head; slanting of the eyelids; a gap between the first
and the second toes; a depressed nasal bridge; relatively small ears, mouth, hands and feet; short
stature; decreased muscle tone and loose ligaments among others. Not every child with Down
syndrome has all of these characteristics and some may have only a few. But other characteristic, if
not appropriately can be including hearing deficits, congenital disease, eye abnormalities, ... Show
more content on Helpwriting.net ...
HISTORY English Physician John Langdon Down first characterized Down syndrome as a distinct
form of Mental disability in 1862, and in more widely published report in 1866.[9] Due to his
perception that children with Down syndrome shared physical facial similarities with those of
Blumenbach is Mongolian race. Down used the term mongoloid derived from prevailing ethical
theory.[10] By the 20th century Down syndrome had become the most recognizable form of mental
disability. Most individuals with Down syndrome were institution zed, few of the associated medical
problem were treated , and most died in infancy or early adult life. With the rise of the eugenics
movement, 33 of the United States and several countries began programs of force sterilizations of
individuals with Down syndrome and comparable degrees of disability. The ultimate expression of
this type of public policy was ''action 7–4'' in Nazi Germany , a program of systematic murder court
challenges , scientific advances and public revulsion led to discontinuation or repeal of such
sterilization programs during decades after World War Until the middle of 20th century, the causes
of Down syndrome remained unknown. However, the presence in all races, the association with
older maternal age, and he rarity of recurrence had been noticed. Standard medical text assumed it
was caused by a combination of inheritable factor which had not been

I Am A For A Boy Diagnosed With Down Syndrome
Unlike my last verbal essay which I was not very passionate about. The topic that I chose for today
is very close to my heart and I am very passionate about it. Why I chose this topic is because I am a
one on one aid for a boy diagnosed with Down Syndrome. His name is Justin and helping Justin is
one of the main reasons I decided to major in social work. I have personally seen Justin blossom
from being placed in an inclusive classroom. An inclusive classroom is when children with and
without disabilities participate and learn together in the same classes. Research shows that when
children with disabilities attend classes alongside peers who do not have disabilities, good things
happen (Stout). When placed in inclusive classrooms, Down Syndrome students blossom
academically and socially from experiencing regular, daily contact with their nonclassified peers.
Academically, Down Syndrome students have the opportunity to blossom and learn more when
placed in inclusive classrooms. Down Syndrome students benefit from being in these classrooms
because they have an equal opportunity to learn the same material as nonclassified students. When
placed in an inclusive classroom every student is taught the same material, but Down Syndrome
students are able to receive a little extra help if needed. This helps the Down Syndrome student to
blossom because they have the opportunity to grow more than they would in a special education
classroom. Peers help Down Syndrome students to blossom by

Steven Johnson Syndrome Research Paper
There are many different types of syndromes and disease in the world today. Steven Johnson is one
of them. This Syndrome is a very rare disorder in the world today. Many persons do not have a clue
in which what this serious is or/and why it occurs. The Steven Johnson syndrome is a disorder of
someone's skin or mucous infection. This occurs when the persons take medication(s) that they are
possibly is allergic to. It's really not the medication but it's like the medication is fighting off some
good cells in the body. Steven Johnson Syndrome is a very serious syndrome or infection. It requires
hospitalization and serious care. The syndrome starts off with flu like symptoms. And it gets worst
as time by without no treatment or care. As the syndrome continue to spread and infect the body
your symptoms get worst and others symptoms occurs. Other symptoms are purple–ish or red rashes
and blisters. That is hard to remove or treat. There are many other symptoms dealing with the Steven
Johnson Syndrome before and after you start the rashes. Before the rashes the person or persons
may experience Sour throat, Burning eyes, fever, etc. when the rashes occurs the following occurs:
Facial swelling, Tongue swelling, Skin pain, A red or purple skin rash. You may also my experience
other types of changes to the body ... Show more content on Helpwriting.net ...
The medications are mostly the reasons to way the serious and critical Syndrome occurs. Some of
these medications are as follows: Penicillin, Tylenol, Advil, Motrin, some medications to treat some
Mental illnesses and Radiation therapy. The Steven Johnson Syndrome can also be caused by some
serious infections or disease like Pneumonia, Herpes, HIV, and Hepatitis. The most common
infection or disease is HIV. If the person has a weakened immune system and is HIV+ can increased
the risk of getting the Steven Johnson. Others are like a family trait. If many people in your family
has or had

Literary Analysis Of Christopher Boone
Literary Analysis Paper
The novel is narrated by the curious voice of Christopher Boone, a 15–year–old child with
Asperger's syndrome. The book follows the life events of Christopher, through whose eyes the
reader explores the world of an Asperger's condition child. The narrative is outline in first person
and gives the reader an insight of the thought processes of protagonist, by following the actions and
choices he makes and displaying the impact they have on their life and that around him. Christopher
sets his purpose early enough to investigate the death of a neighbor's dog, which was killed by a
pitchfork. He heads the advice by his teacher, Siobhan and writes the detective work in a detective
novel style. Christopher, in his narrative, ... Show more content on Helpwriting.net ...
(2004). Asperger syndrome from childhood into adulthood. Advances in Psychiatric treatment,
10(5), 341–351.
Draaisma, D. (2009). Stereotypes of autism. Philosophical Transactions of the Royal Society B:
Biological Sciences, 364(1522), 1475–1480.
Greenwell, B. (2004). The curious incidence of novels about Asperger's Syndrome. Children's
Literature in Education, 35(3), 271–284.
Haddon, M. (2007). The curious incident of the dog in the night–time. National Geographic Books.
Haller, B. (2004). The Curious Incident of the Dog in the Night–time. Disability Studies Quarterly,
24(4). Thistlethwaite, J. (2003). The Curious Incident of the Dog in the Night–time. BMJ,
327(7418),

Johnson Munson Syndrome Analysis
Johnson–Munson syndrome is a rare syndrome identified by missing abnormal vertebrae, fingers
and toes and various deformities of the heart, lungs, intestines, pancreas and intestines. Ophanet a
consortium of European partners defines a condition as rare. In the US population, less than 200,000
people can possibly be affected by Johnson Munson Syndrome or second type of Johnson Munson
syndrome. (Orphanet 2015)
Johnson Munson syndrome will start within the DNA from the formation of the fetus at birth. There
are birth defects that cause the variety of disfiguring parts of the body. There for the limbs may not
be of proper size and these could consist of a toe or finger missing. The toes and fingers can also be
grown together, arms, and legs may not be fully developed. As of today, there is one known risk
factor that has been found within the first year of the child's ... Show more content on
Helpwriting.net ...
A few examples are Home blood pressure hypertension test, heart rate monitors, heart ECG,
cholesterol testing, lung function, bladder testing, urinary tract infection test, home cystitis test,
home kidney test, home urine protein test for the kidney, home prostate cancer test, hormone test,
libido test, menopause testing, andropause test, hepatitis test, liver test, sexually transmitted disease
test, stomach ulcer test, colorectal cancer test kits, fecal occult bleeding test kits, food allergy test,
food intolerance testing, water testing, lead poisoning test and heavy metal poisoning test. There are
also undiagnosed with Johnson Munson disease that include chrohn's disease, celiac disease,
heartburn, ulcerative colitis, inflammatory bowel disease, irritable bowel syndrome, carcinoid
syndrome, and pancreatitis. Looking at Johnson Munson syndrome it can be of use to consider the
disease that might have been misdiagnosed. Although another condition that might be of relevance
to diagnose might exist as well (Right Diagnosis,

Cornelia De Lange Syndrome
Cornelia de Lange Syndrome typically presents with a constellation of distinctive features affecting
several different parts of the body. There is a wide degree of variation between individuals with the
disorder in the presentation and severity of symptoms; however, the features described below
represent a typical presentation. Slow growth during both fetal and post–natal development is a
characteristic feature of the disorder. Approximately 90% or more of patients display delayed
skeletal maturation, and about 50% were noted to have intrauterine growth retardation (2). Because
of this, individuals with Cornelia de Lange syndrome tend to be short in stature, with height and
weight falling below the fifth percentile throughout life (3). ... Show more content on
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Other limb issues such as small hands (micromelia) and incurved fifth finger (clinodactyly) are
prevalent (3,1). In addition to the above core features, the syndrome tends to have effects on several
major systems of the body. For example, sensorineural hearing loss impacts 80% of children with
CdLS; approximately 40% are severely affected (3). Opthalmological issues, such as myopia (near–
sightedness) and nystagmus are also common. Patients may also have inflammation of the eyelid of
droopy eyelids (ptosis) (1). Neurological issues can include sleep problems and seizures.
Approximately 25% of diagnosed individuals experience seizures (3), which can usually be well
controlled with standard medical intervention (4). Neuroimaging has shown characteristic features
such as enlarged ventricles at the basal cisterns, undergrowth of the brainstem and cerebral vermis,
and atrophied white matter especially in the frotal lobes. High pain tolerance caused by problems
with peripheral neuropathy have also been reported (4). Cornelia de Lange Syndrome can also
include cardiovascular concerns. Congenital heart disease occurs in approximately 25% of
individuals with the disorder. The most common

Savant Syndrome Chapter Summary
In this chapter, author talks about couple of people with savant syndrome and have extraordinary
skills. People like Eddie who had multiple disabilities as well as blind. But he has spectacular
musical ability. Also Brittany maier who was 16 and was blind from birth with limited verbal skills,
but astonishing pianist and composer. Kodi Lee is who has exceptional vocal and piano skills. Wen
Kuei who was blind but he has exceptional skills on musical. It is believe that cause of blindness
occur often in musical savants. Blind savants suffer from septic optic dysplasis that cause optic
nerve hypoplasia, pituitary abnormalities and the absence of the spectrum pelludium and corpus
callosum. Author talks about the foreign accent syndrome (FAS), ... Show more content on
Helpwriting.net ...
Although he never had an art lesson, but he can sculpt animal. For him, one glimpse is enough to
sculpt. His brain is like a digital camera that takes a picture and stored. He became prodigious
savant after he injured his head as a child that slow down his development affecting his cognitive
ability, vocabulary as well as speech. Sculpting was his way to communicate. His art skills have
improved along with his speech and vocabulary, social and daily living skills. His sculpting technic
are quite impressive and his works are display in Driscol Gallery in Aspen,

Sleep Apnea Theory
Epidemiology: Obstructive sleep apnea is becoming more prevalent in adults and children in our
society. Obstructive sleep apnea is undiagnosed mostly in women being 92% and 80% in men. The
estimated prevalence in women is 2% and in men is 4%. A study was done by the University of
Pennsylvania revealing that the prevalence in women was 4% and 9% for men. Another study called
The Wisconsin Cohrt study showed that people who are 30 to 60 years old, the prevalence is 9–24%
for men and 4–9% for women. Although Obstructive sleep apnea is less certain in children, in the
recent years they have seen an increase of cases of children who have sleep apnea. This is due to the
fact of children being obese or to their counterparts. Although there has been an increase of cases
this might be an effect of being sleepy or hyperactive. Nonetheless as a result of a recent study in
2007 they have concluded that 6% of children who are teenagers. There was a done by The
California University of ... Show more content on Helpwriting.net ...
There was a community sample performed to see what was the percentage of people who are 65
years or older. After the tests they found out that the prevalence was 65%. After 65 years old there is
no big difference on the topic of Obstructive Sleep Apnea. According to Community studies The
male to women is 2–3:1. The body patterns of males including body fat distribution makes them
more inclined to get Obstructive Sleep Apnea. Women are not only less likely than men to get
Obstructive Sleep Apnea, but also are less likely to get diagnosed early in the disease process. It has
been proven that the rates of survival are lower for women due to the fact of they get the diagnosis
too late. Studies also show that women have a higher prevalence to get Obstructive Sleep Apnea
after Menopause.

Literary Analysis Of Plot In 'The Memory Keeper's Daughter'
Section 1: Demonstrate understanding of the literary techniques employed by the author in the
selection.
Plot
Dr. Henry and Norah were expecting a baby boy, and when Norah went into labor; she found out
that her baby boy was healthy, but she also had a baby girl that had a heart defect. After the twins
were born, she didn't remember having the twins. Dr. Henry told his wife that was barely awake,
that their daughter had died, but what Norah didn't know is that her daughter was alive with an
illness, and Dr. Henry didn't want to put up with that. Their daughter, Phoebe was taken care of by
Caroline, the nurse. Caroline was supposed to take Phoebe to an institution but decided to raise her
on her own. David found out that Caroline wasn't taken to the institution, and told her to do the right
thing. Caroline left Pittsburgh with Phoebe for a fresh start. At the end, they reunited with Phoebe
and Caroline and Norah remarried in the final few pages of The Memory Keeper's Daughter. David
went through the down syndrome thing with his sister, June, that's why he gave Phoebe up.
Structure/Form
Chapters go back and forth between David and Norah, and the family of Caroline and Phoebe. The
book covers 25 years in 400 pages. The structure was an unnatural gulf between David and Norah,
and their missing family member (Phoebe). The fragmented structure represents the fragmented
nature of their lives, and to keep things fast–paced. The story forms as the lives of these characters
change

Goldman Fristoe Case Study
Before I gave the Goldman Fristoe to Lauren, my client, I asked why she they wanted to bring her in
to the Butler University Clinic. The parents said that her preschool teacher had a hard time
understanding her in class and suggested to take her to a speech pathologist. Lauren spoken
language is English and there were no prior medical issues. Therefore, I decided to give Lauren the
Goldman Fristoe to see what phonemes she struggled with. Since Lauren is 4 years, 10 months and
17 days old, I gave her the sounds–in–words section then sounds–in–sentences section for ages 4:0–
6:11. During the sounds–in–words section, I showed Lauren a series of pictures and asked her what
each picture was. Sometimes I would point out specific out in the picture and asked her what that
certain object was. This section focused on ... Show more content on Helpwriting.net ...
I felt I did a decent job at giving the Goldman Fristoe to Lauren. I read the directions and tried to
make taking the test fun. I used the directions whenever Lauren did not say the word I wanted to
hear and did not talk monotone. I From the view of a client, I felt taking the Golden Fristoe was
difficult. It was difficult to mispronounce phonemes within words. Though I practiced
mispronouncing my phonemes, when I came to taking the test, I still struggled mispronouncing
them. It was easier to mispronounce phonemes in words rather than in sentences. I also found it hard
to mispronounce phonemes during the stimulability section of the test. I felt one thing I could have
done to make the test giving process better is being more fluent when giving the test. One thing I
could have done to make taking the test easier is mastering my incorrect phonemes. While I was
taking the test, I was trying to fronting and stopping. I thought scoring the Golden Fristoe was fairly
easy. All I had to do was add up every phoneme Lauren mispronounced in each section for a raw

Dear John
Your Dad Loves You, I Can Tell, Even If You Can't Jael Zimmerman Westmoreland County
Community College Abstract Dear John by Nicholas Sparks uses two main characters, John's father
and Tim's brother Alan, to express the symptoms and complications of the psychological disorder
Asperger Syndrome. This disorder is considered a form of autism. People with this disorder will be
passionate about one or more topics, but will struggle with daily tasks. The novel provides an
extended metaphor through John's father through his obsessive interest in his coin collection, and is
difficulty in forming a relationship and communicating with his son as he attempts to raise him on
his own. Evidence from his routine schedule and his trouble in controlling ... Show more content on
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She has started a program for children with autism, and owns a farm where she encourages them to
ride horses, and help them have fun and to aid with their illness. John sells his dad's entire coin
collection to help find a cure for Tim's illness (Sparks, 2006). The story ends with the saying that
when you really love someone, you think about their happiness, more than your own. The novel
presents characters that represent the symptoms and complications of Autism and Asperger
Syndrome. Behavior is dysfunctional, when it interferes with a person's ability to function on a daily
basis (Davis&Palladino, 2007). Some of the more common characteristics of Asperger
Syndrome include difficulty in communication, problems expressing feelings, devotion to routine,
and obsessive interests in one or more topics (Jaffe, 2010). John's father, Mr. Tyree conveys
indication of the psychological disorder in his behavior throughout the entire novel. Even though
Mr. Tyree has raised John on his own, during the novel, there is not much communication between
the two. As a teenager and even as a adolescence, when John was home his father would greet him
the same way every morning simply saying good morning. They would eat breakfast and dinner in
silence. When he tried to discuss Savannah in a conversation, he didn't know what to say. The fact
that John could never talk to his

Angelman Syndrome
There are many diseases and syndromes that occur in the developmental stage of human
development. One of the many syndromes is Angelman syndrome. When this syndrome was first
discovered by Harry Angelman, it was known as "happy puppet syndrome". This syndrome is not
typically diagnosed at birth, but can also be diagnosed from the ages of one to six. This syndrome is
a neuro–genetic disorder that occurs in one in 15,000 people. Because of its rareness, this syndrome
is often misdiagnosed as autism or cerebral palsy. Make thesis– Angelman syndrome is caused by a
defect in the UBE3A gene, has various symptoms, that can be misdiagnosed, and patients will live
with lifelong treatment. The are various causes of Angelman syndrome, but the main cause ... Show
Angelman syndrome can be diagnosed within the first year of the life if the abnormalities are
noticed and investigated, but the disorder is more often diagnosed between 1 and 4 years of age as
the child's abnormalities become more clinically apparent (Bevinetto). In order to confirm the
diagnosis, a blood test must be done to look at the child's genetics (Angelman). Then, a combination
of genetic test can reveal the chromosome defects. There are three different defect tests may reveal:
parental DNA pattern, missing chromosome, or gene mutation. Parental DNA pattern test screens for
three of the four genetic defaults that cause this syndrome. To find out if the chromosome is missing
either a fluorescence in situ hybridization (FISH) test or a comparative genomic hybridization test
(CGH) can show if portions of chromosomes are missing. It is rare if Angelman syndrome occurs
with only a gene mutation. This happens when the UBE3A gene is present and active, but mutated.
A UBE3A gene sequencing test is used to look for maternal mutation (Mayo). After the diagnosis is
complete, treatments are discussed with the patient and their

Asperger 's Syndrome Of Children
Asperger's Syndrome in Children
Submitted in fulfillment of the extra credit requirement
For PSYC 4176: Advanced Child Psychology
Louisiana State University
By
Emily France
April 2, 2015
Abstract
Asperger's Syndrome is a pervasive developmental disorder that often presents itself in children
during the elementary years. It is characterized by deficits in social interactions, normal developing
language, fixation with specific objects, and average or above average intellectual functioning. It is
highly debated over whether Asperger's Syndrome is qualitatively different than high functioning
Autism. Symptoms of Asperger's Syndrome will present themselves in a variety of ways that are
unique to each individual child. Within ... Show more content on Helpwriting.net ...
The children were extremely original in their language and thoughts, but struggled with social
interactions (Stoddart, 2005, p.14). When interacting with people, their language and relations were
abnormal from those of their age–level peers (Stoddart, 2005, p. 14). The children seemed distant
and indifferent towards people, but extremely interested and invested in objects (Stoddart, 2005, p.
14). He described attachments and fixations with objects that were debilitating and interfered with
normal every day functions (Stoddart, 2005, p.14). Asperger had a positive view on these children.
He recognized that these qualities could present some difficulties, but he instead focused on the
strengths of these abnormalities (Silverman & Weinfeld, 2007, p. 3). Asperger believed that the
characteristics he observed would lead to strengths across the lifespan that would not be present in a
normal–developing child (Silverman & Weinfeld, 2007, p. 3). Asperger believed that these children
should and could be educated, so he built a school for them (Silverman & Weinfeld, 2007, p. 3).
This school was bombed during World War II, which possibly led to the delay of his studies
spreading to the west (Silverman & Weinfeld, 2007, p. 3).
Lorna Wing brought attention to Asperger's work in the 1980's with her research in London
(Stoddart, 2005, p. 14). Her research agreed with Hans Asperger's in many ways, however she also
stated that signs of

Cri-Du-Chat Syndrome Research Paper
Cri–du–Chat (cat's cry) Syndrome is a rare chromosomal disorder that is caused by the deletion of
genetic material on chromosome 5. Due to this, this syndrome has an alternative name, known as
5p–, or 5p minus syndrome. Although this genetic defect is able to be diagnosed, the cause of the
deletion on the chromosome is unknown. Almost all cases of the Cri–du–Chat Syndrome are found
to have no relation with family members or previous generations. This syndrome is generally not
inherited, as the deletion occurs randomly during meiosis (the formation of the gametes). In about
90% of people who have this condition, the deletion is completely random and is not inherited. The
remaining 10% of affected people inherit a chromosome with a deleted section from an unaffected
parent. This is because the parents' balanced ... Show more content on Helpwriting.net ...
This deletion can occur through a variety of genetic arrangements, in the form of unbalanced
translocation, ring chromosomes, interstitial deletion, and inversion. The main symptom of
individuals with Cri–du–Chat is that at a young age, they have a high pitched cry, that resembles
that of a cat. This cry generally becomes less noticeable as the individual ages. Some of the other
symptoms of Cri–du–Chat Syndrome are mental retardation, hyperactivity, delayed development,
small heads, round faces, low nasal bridges, widely–spaced eyes, low birth weight, and weak muscle
tone. Since the size of the deletion of the genetic material varies between each affected person, these
individuals can all show slightly different symptoms and levels of intensity with these symptoms.
Individuals with this syndrome may come across feeding issues due to difficulties in swallowing
food and sucking in liquids. They also sometimes lack sufficient communication and verbal skills,
and face delays in the progress of learning to walk. There is no cure for Cri–du–Chat Syndrome as
of

Reflection On Velocardiofacial Syndrome
Tierani Richardson Reflection 15 Content: Our group was assigned velocardiofacial syndrome
(VCFS). I was excited to receive a syndrome to which I had not been exposed. I was assigned
etiology, history, and incidence/prevalence. I learned that VCFS originates from the Latin words
"velum" which means "palate," "cardia" which means "heart," and "facies" which means having to
do with the face. It is the most common syndrome associated with cleft palate! Additionally, VCFS
is an autosomal dominant condition. This means that once a person is recognized as having VCFS,
they have a 50 percent chance of passing the syndrome on to their offspring. VCFS is characterized
by a small deletion of chromosome 22, more specifically in the region of 22q11.2. This deletion
results in about 30 genes becoming absent from chromosome 22. Two genes in particular–COMT
and TBX1–are associated with VCFS (not all genes that cause VCFS have been identified).
However, I am not sure why these genes are involved. I tried to research the reason, but could not
find a plausible explanation. I also learned that more often than not, neither parent of a child with
VCFS has the deletion of 22q11.2. This means that the condition is NEW in 93 percent of offspring.
The good news is that the chance for the couple to produce another child with VCFS is close to zero.
The deletion occurs as an accident when either the egg or sperm is being formed, OR early in fetal
development. Angelo DiGeorge, MD, is one of the people

Gulf War Syndrome Essay
Gulf War Syndrome
One part of being an American, is giving yourself to your country when deemed necessary. In 1991,
the United States took action in the Gulf War, where many US solders were sent. In fact, a total of
697,000 solders took part in the Gulf War. And of that amount, 6% (about 45,000) veterans have
reported an ailment related to this war. Much chaos arose from these sicknesses, and from this a
syndrome was born. The syndrome is called the Gulf War Syndrome. Wether this is myth or not has
been throughly researched, but how can one claim 45,000 veterans to be falsely accusing an ailment
they believe to be at fault of the Gulf War?
There are many different sides of these syndrome, and much hype about who's right and ... Show
These scenario may seemed far–fetched, but unfortunately there are many more stories as
outrageous and even more so. Another unfortunate symptom is birth–defects. 67% of the Gulf War
veterans' babies are born deformed.
Humans weren't the only ones which were effected by this syndrome. What were once battle fields
for the Gulf War, were later used for agricultural purposes. Sheep particularly were raised in these
areas. Many sheep died mysteriously, and other sheep became very sick. To prevent more sick
sheep, agricultural organophosphates are carefully established on the known degree of toxicity of
each compound. The organophosphorous used is Bayer 21/99, which is a popular compound that
inhibits treated animals from the skin and digestive tract. Sheep are also more susceptible to
poisoning then cattle and most other emaciated animals. Pre–treatment consisted of weighing, ear
tagging, and the collection of blood samples for a baseline red cell count. It is shown that animals
which have been treated have a much higher tolerance to poisons and a less likely to have more
ailments. Symptoms include: Irregular gait with generalized muscular weakness and severe diarrhea.
Slight increase in salivation and isolated diarrhea. Irregular gait with generalized muscular weakness
and severe diarrhea.
Much of the GULF WAR SYNDROME hype arose because of

Many characters in movies, television shows, and novels...
Many characters in movies, television shows, and novels have been portrayed or have been hinted to
have a psychological disorder. Some examples are Ariel from The Little Mermaid, who has
obsessive–compulsive disorder and is a hoarder, and Mike from the animated series Total Drama,
who has dissociative identity disorder. This phenomenon has become more prevalent in popular
media. These characters appear in all types of genres: psychological thrillers, comedies, mysteries,
musicals, and more. The Big Bang Theory is a television sitcom that features a character that has
many symptoms of a psychological disorder called Asperger's syndrome, and this character is
Sheldon Cooper. Asperger's syndrome is a psychological disorder that "affects ... Show more content
on Helpwriting.net ...
Due to his lonely childhood, he is very awkward and walks and talks in abnormal ways. He is
completely oblivious to humor and once tries to create an equation for humor so that he could better
understand it. Sheldon also has obsessions with Star Trek, Star Wars, flags, comic books, and trains,
his main obsession. Even though Sheldon is not confirmed to have Asperger's syndrome, some of
the myths about it have been incorporated into the show and Sheldon. Asperger's syndrome and
obsessive–compulsive disorder are similar, but they are not the same thing. People can have both
Asperger's syndrome and OCD. Asperger's syndrome is more common in males, and OCD is more
common in females. On The Big Bang Theory, Sheldon has obsessive–compulsive tendencies along
with symptoms of Asperger's syndrome. He has his designated spot on the couch, does laundry on
certain nights, and knocks on people's doors three times and says their name three times. Sheldon
exhibits the myth that he makes people very angry and irritated when he interacts (Hutten). Because
Sheldon is awkward or uninformed about social situations, he can easily upset and anger people. For
example, in one episode Sheldon insults an African American woman, the head of the Human
Resources Department at the university where he works, by calling her a slave and giving her the
novel Roots. Because Sheldon Cooper is never confirmed to have Asperger's syndrome, no specific
treatments are explored for him for

The Article Is Titled “Communication Modality Sampling
The article is titled "Communication Modality Sampling for a Toddler with Angelman Syndrome"
by Jolene Hyppa Martin, Joe Reichle, Adele Dimian, and Mo Chen. The authors explored three
modes of communication, vocal, gestural, and graphic, with a young child with Angelman
syndrome. The researchers investigated which mode of communication would be the most effective
and efficient for the child.
Angelman syndrome can cause cognitive, communication, and physical disabilities. It is a disorder
that affects around 1 in 10,000 births and for the majority of the cases, the cause is genetic.
Angelman syndrome can be caused by an abnormality in chromosome 15. Previous research on
Angelman syndrome and the different communication modes is lacking. ... Show more content on
Helpwriting.net ...
This symbol is taught in gestural, graphic, and vocal mode. The modality sampling has many
advantages, one of the most important being that it provides important intervention resources.
The main purpose of this study was to compare the efficacy of graphic and gestural modes of
communication with a toddler with Angelman syndrome (Martin, Reichle, Dimian, & Chen, 2013).
The participant was Adam, a 21–month–old male with Angelman syndrome. Before the study
started, Adam was assessed in communication, cognition, and fine and gross motor skills. Adam did
not engage in vocal imitation or turn taking. His mother reported that Adam would sometimes
vocalize to get her attention, he would also protest, request, and express excitement. Adam's fine
motor skills were delayed, but he had adequate movements to produce gestures for the study.
Before the sessions started, the three researchers went through a role–play training. This was done to
increase reliability and interobserver agreement between the researchers. The 44 sessions occurred
at the participant's house or at his day care center. The first session was a baseline probe and the rest
of the sessions were divided into five phases. The sessions were held two times per week for five
months. The materials for the study included three objects or activities that Adam liked or

Angelman Syndrome : The Happy Puppet Syndrome
According to the US National Library of Medicine (2017), Angelman Syndrome, also known as
Happy Puppet Syndrome is a "complex genetic disorder that primarily affects the nervous system."
Angelman Syndrome occurs when there is a change to the E3 Ubiquitin Protein Ligase Gene
(UBE3A) located on chromosome 15.
Angelman Syndrome was first discovered by Harry Angelman, a Physician in 1965, when he
witnessed three young children who represented similar symptoms. They all had bright, happy
personalities, along with stiff movements, lack of speech and seizures. While in Italy for the
holidays, Harry Angelman visited a museum that showed a picture of a puppet that had the same
physical appearances as his patients. He diagnosed his patients with Happy Puppet Syndrome,
which would later be known as Angelman Syndrome. In 1987, Ellen Magenis, who is also a
physician, identified children who seemed to have Prader–Willi Syndrome, a similar genetic
disorder to Angelman Syndrome. The difference between Angelman Syndrome and Prader–Willi
Syndrome, is that Angelman Syndrome can be caused by the deletion of the maternally derived
chromosome 15, while Prader–Willi Syndrome is the deletion of the paternally derived chromosome
15.
Symptoms of Angelman Syndrome include, but are not limited to sleeplessness, hyperactivity, short
attention spans, feeding difficulties and sensitivity to heat. It is also common for people with
Angelman Syndrome to have developmental delays, lack of speech,

Munchausen Syndrome Research Paper
Munchausen Syndrome, a mental disorder where the patient seeks attention or sympathy through
fictitious ailments. Coined by Dr. Richard Asher after a German nobleman named Karl Friedrich
Hieronymus, Baron von Munchausen of the 1700's. Baron von Munchausen was a military man who
returned from war telling outrageous stories of his travels and adventures he endured during his time
away from home. In 1951, Dr. Richard Asher applied the term Munchausen to patients who traveled
from hospital to hospital seeking medical attention for fake, exaggerated or self–induced injuries. In
this paper we are going to discuss, A: The symptoms of Munchausen syndrome. B: Munchausen
syndrome by proxy. And C: The importance of quickly diagnosing Munchausen's disease. ... Show
Most often Munchausen's by proxy is between mother and child, or caregiver and child. The
perpetrators of this form of Munchausen's receive the attention they crave by playing the hero role
or ultra–caring parent while also assuming the sick or injured role by proxy. Munchausen's by proxy
is often undetected because it appears as a form of neglect or child abuse. Munchausen's syndrome
by proxy may sometimes be described as a mental disorder or simply as abusive behavior. In regards
to either form of Munchausen's syndrome, neither appear in the "Diagnostic and Statistical Manual
of Mental Disorders" ("DSM–IV–TR") under that name but are categorized under "Factitious
disorder." Because of the complexity in diagnosing Munchausen's syndrome by proxy, doctors under
suspicion sometimes attempt a "separation test." In this test the doctor will observe the proxy victim
in absence of the care giver. Quite often the symptoms will disappear. Care must be taken when
conducting such tests because if the doctors assumptions are wrong, the seriousness of the child's
illness may have been compromised putting the child's life further at

The Genetic Testing Controversy Essay
A lot of controversial issues present themselves in psychology. Two topics that I will be discussing
in this essay are the controversy over genetic testing and what things would be like without genetic
testing. I will be describing what genetic testing is, and how it can affect an individual's family life. I
will be discussing the benefits of genetic counseling, as well as the positives without genetic
counseling, and how this issue is debated in a psychological view. Genetic testing, can affect a
person's life in many ways. Genetic testing is a type of medical testing that identifies changes that
occur in chromosomes, proteins, and genes. These changes that occur can be associated, and often
are associated with inherited ... Show more content on Helpwriting.net ...
As her husband was fighting in the war, there were troubles that this wife had to face with their
child. She did genetic testing on her daughter to find out that her daughter happened to be diagnosed
with Rett syndrome. Rett syndrome is a neurodevelopmental problem that occurs in the nervous
system (Tarquinio). The wife stated "I think as a military spouse you learn to adjust easily and
expect that your life might change at any given moment, but nothing can prepare you to learn that
the change in life is coming from your child." Since the wife was able to know that her daughter was
diagnosed with the syndrome, she was able to do research to help with what she needs to do
(Steveton). This goes back to family planning and how genetic testing can be beneficial for families.
Not only are there benefits with genetic testing, but there are benefits by not going through genetic
testing. Genetic testing can be costly, and therefore will be less expensive by not following through
with the tests. Genetic testing is usually not covered by insurance; therefore, many families would
have to decide if the costly payments are worth their budget. More than one test may have to be used
to detect if there is a disease taking course. Back to the military wife, two of her daughter Riley's
tests came back negative. At first, her daughter was diagnosed with developmental delays. Not only
did she go through doing genetic testing, but she also did an MRI. Both of these tests didn't

Memories Of The Gulf War Syndrome
9
MEMORY LOSS IN GULF WAR SYNDROME
Katherine Krishun
What Causes Memory Loss in Gulf War Syndrome? Chemical Exposure or Stress?
PSY 101/112
10/24/2016
Gulf War Syndrome is a chronic multi symptom illness affecting 250,000 of the 697,000 1991
Desert Storm Gulf War veterans. Iraq and Afghanistan war veterans may also suffer from this
syndrome. The Veterans Administration "refers to these illnesses as "chronic multi symptom illness"
and "undiagnosed illnesses". We prefer not to use the term "Gulf War Syndrome" when referring to
medically unexplained symptoms reported by Gulf War veterans. Why? Because symptoms vary
widely" (Gulf War Veterans Medically Unexplained Illnesses, 2016). The illnesses included in this
syndrome are: chronic fatigue syndrome, fibromyalgia, functional gastrointestinal disorders, and
undiagnosed illnesses including fatigue, cardiovascular disease, muscle and joint pain, respiratory
disorders, headaches neurological and psychological problems, and sleep disorders.
Research is being done on the correlation of combined chemical exposure plus stress and their
effects on memory. Many veterans suffer from PTSD and some researchers believe that the Gulf
War Syndrome (GWS) symptoms are in response to the stress associated with PTSD alone. Other
researchers believe that along with stress, there are neurological deficits linked with chemical
exposures.
Prior to entering the theatre of operation, veterans were given

Lejeune's Syndrome Research Paper
Genetic Disorder that Gives the Cry of a Cat The genetic disorder named "cri du chat" is a partial
depletion of chromosome 5p. Also known as " Lejeune's syndrome" as first described by Jerome
Lejeune in 1969. The name "cri du chat" is a French term, which means cat–cry or call of the cat,
because of how affected children have a kitten like cry. It affects about 1 in 50 000 children born,
predominantly inherited by females by a 4/3 ratio. Although this particular symptom has been
named after, the symptom of the cat like cry may be lost past age 2. There are other symptoms of
this disorder. Other symptoms may include: Feeding problems; Low weight and growth; Speech
problems and motor delays; Behaviour problems; Abnormal facial features; Mental

Stockholm Syndrome
This documentary caught my attention right from the opening lines. People, in general, do not like
to admit when they are wrong, so when the narrator began by claiming that the entire set of beliefs
he had grown up with and lived his life by were wrong and "untrue" it made me stop and consider
how that would affect a person. To have your entire way of thinking be proven invalid would be an
unsettling situation to put it simply. I could not begin to imagine how that would feel, but I tried to
keep this thought in mind as I continued with the rest of the documentary as it explored complex
ideas involving education, employment, and obedience. As someone who is pursuing a higher
education by attending college, I believe education is incredibly ... Show more content on
Helpwriting.net ...
I can't say that I honestly enjoyed watching it, but then again that is not the point of a documentary
such as this. This documentary, although not the most exciting to watch, forces you to constantly
evaluate and consider the information being presented to you. There were times I would have to
rewind just to give my thoughts a second to catch up, and in that sense, the film fully accomplished
its goal. In discussing complicated ideas such as education, employment, and obedience it showed
me just how narrow my scope of the world is, and I think I can better understand what the narrator
meant and how he felt when he said: "almost everything I was brought up to believe turns out to be

Williams Reflection
Tierani Richardson
SP Reflection 16
Content: Group one presented over Williams Syndrome. Williams Syndrome is a genetic condition
that is caused by a deletion of 26–28 genes on chromosome seven. The more genes deleted, the
more severe the characteristics will be. The deletion is also present from conception due to an
abnormality of the egg or sperm cell. The syndrome is named after John C. Williams. However,
Alois Beuren is also credited for research on Williams, which is why it used to be referred to as
Williams–Beuren Syndrome. Williams occurs in less than 20,000 people in the United States! That's
incredibly rare! It is also interesting to know that the disorder affects males and females equally.
Some key characteristics of this ... Show more content on Helpwriting.net ...
It was also interesting to see the support groups and foundations of Williams Syndrome across the
world including places like New Zealand, Australia, Hungary, and South Africa.
Process: I think group one was well organized and spoke extremely well. I enjoyed their
presentation. I liked the presentation overview in the beginning that explained what we would be
introduced to and who would be speaking, this was a great organizational touch! I loved the first
overview video the group showed. It explained the syndrome wonderfully and was interesting to
watch. I like how Tatum pointed to the chromosome picture and explained the crossover. However, I
think she should have turned the other way so her voice would have projected to the entire class.
She also did a great job with the pronunciation of all of her names and terms. I like that she took the
time to perfect this detail. I also liked how she bolded the "main" points of her slides. It was a great
way to make those points salient. Karlee also spoke well and I liked how she defined affinity and
circumlocataion. I did not like how she was the only one wearing jeans. She looked great, but I think
she should have worn dress pants to match the rest of her group. Sydney did well, however, I think
her portion was too brief. For example, I think she should have given examples over the different

Down Syndrome Speech Outline
. When parents/ families find out they are going to have a child, or do have a child with Down
syndrome, it is a life changing experience that most need guidance with. 1. The Center for Disease
Control and Prevention state that, "Down syndrome continues to be the most common chromosomal
disorder. Each year, about 6,000 babies are born with Down syndrome, which is about 1 in every
700 babies born." 2. Heart Problems: The Center for Disease Control and Prevention also state,
"About 50% of all babies born with Down syndrome are also born with a congenital heart defect.
Babies with Down syndrome can be affected by a wide variety of heart defects. Many of these
conditions will need surgery, while some milder heart defects might go away on their ... Show more
content on Helpwriting.net ...
Positive: The Down Syndrome Information Alliance states that, " We envision a community where
people with Down syndrome are empowered, respected as individuals, and accepted as valued
participants in neighborhood schools, community activities, and the business world."
Transition: Now the real question is, what can you do to help?
III. Conclusion (Call–To–Action) A. Review of main points: Today I have discussed why the Down
syndrome community needs support, how the DSASTX provides means of support, and how this is
important. B. Action Statement: Today, I encourage all of you to either donate your money, or time
to this organization. Without the finical support, many families would not be able to afford medical
bills, education, or be able to attend programs for their children or family members. By volunteering
you become actually involved on a physical level. I believe that actually volunteering does a whole
lot more than donating, and as an Aggie Selfless service is what were suppose to do. By
volunteering at the Down syndrome Buddy Walks, or camps and programs put on by DSASTX you
can personally involve yourself with this organization and make a difference in the lives of many
people. C. "I Have a Dream... someday my son, Zyon and ALL individuals with disabilities will be
seen as HUMAN

Asperger?s Syndrome and Instructional Intervention Essay
Asperger's Syndrome and Instructional Intervention
Asperger's Syndrome (AS) is a pervasive developmental disability first identified in 1944 by Dr.
Hans Asperger, an Austrian pediatrician. However, since his paper was written in German and
published during World War II, his findings were not well known in the United States and in other
non–German speaking countries. In 1981, Dr. Lorna Wing, a British researcher, brought AS to the
attention of the English–speaking world. In addition to summarizing Asperger's findings, she also
pointed out the similarities between AS and autism, raising the question: Are they the same disorder
or two separate ones (Ozonoff, Dawson, & McPartland, 2002)? It was not until 1994 ... Show
Many children with Asperger's are first diagnosed with attention deficit hyperactivity disorder
(ADHD). They may have problems with social interactions, but their main difficulties are
inattention, hyperactivity, and impulsivity. It is not until the inappropriate social behavior becomes a
greater concern that they are diagnosed with Asperger's (Watkins, 2000).
Children with AS often have behavioral and emotional problems connected to their deficient social
skills. These often involve feelings of stress or loss of control (Myles & Simpson, 2002) and
these behaviors can range from simply annoying to highly disruptive behaviors (Safran et al., 2003).
In order to help students with AS, interventions must be used that target improving social
understanding rather than trying to change certain behaviors in certain situations. Improving the
social understanding can be addressed by teaching appropriate social skills. These social skills may
include problem solving, conversation skills, anger control, identifying and managing feelings,
dealing with stress, and organizational skills. A school psychologist may assist by providing direct
social skill instructions to the student and training parents and teachers in strategies to use. Some of
these strategies include social stories, comic strip conversations, and social autopsies. In addition,
teaching students the "hidden curriculum" or "unwritten rules of conduct" are important parts of
social skills teaching

Clinician Intervention Case Study
As addressed in the previous section, assessment needs to be very individualized towards the patient
and their specific needs. Therefore, with intervention, the same process and considerations should be
maintained. If a clinician is going to individualize an assessment specifically towards a client, then
in order to work on the areas identified, the intervention plan must reflect the results of the
assessment. Every individual varies greatly, and with Noonan Syndrome, it is no different. Even
though specific characteristics are identified, each patient will present with different degrees and
attributes, if they even present with any at all. Intervention needs to be specifically designed for the
individual and their strengths and weaknesses. ... Show more content on Helpwriting.net ...
The caregiver is a major component of the intervention, and that cannot be forgotten when
determining plans for intervention. The caregivers are going to be the main adults interacting with
the child and ultimately implementing the strategies to excel the development of their child.
Therefore, the SLP needs to make sure that they are addressing the concerns of the caregivers
throughout the intervention process. A clinician should view the caregivers as an important
component in the intervention process, comparable to the client. If the caregiver mentions skills that
they wish their child to improve upon, or want certain issues the child may have addressed, then the
clinician needs to make sure to target those issues and address them accordingly. Secondly,
caregivers are a huge resource that the clinician can use to enhance the productivity of the
intervention. The caregiver can provide insight into the interests of the child, how to interact with
the child, or give the clinician pointers as to what to avoid during interactions. (Ritzman,

Autism Spectrum Disorder And Autism Essay
Autism and Asperger's are two syndromes that are now looked as being part of the 'Autism
Spectrum Disorder'. Asperger's is on the high functioning end while Autism is on the low
functioning end. Before the 'autism spectrum' was created, in nineteen forty–three and nineteen
forty–four, a psychiatrist named Leo Kanner and German scientist named Hans Asperger discovered
Autism and Asperger's. Their research included looking at cases of children who were different and
had qualities of aloneness, obsessiveness, and trouble with social interactions. Leo Kanner and Hans
Asperger helped others understand children who were different and helped us today as we used their
research to further the identification of Autism Spectrum Disorder. Leo Kanner was born in Austria
in 1894 but he went to school in Berlin. He came to the United States in nineteen twenty four where
he received a position as an assistant doctor at a hospital in South Dakota. In 1930, he moved to
Johns Hopkins hospital, where he founded the first child psychiatry clinic in the country. He then
wrote his first book in 1935 called Child Psychiatry that defined his definition of child psychiatry
and what he found in his research. In 1938 he started his research on eleven children and started to
write his next article and first described the syndrome of infantile autism ("LETTER TO THE
EDITOR Asperger (1906–1980) and Kanner (1894–1981), the Two Pioneers of Autism") Leo
Kanner wrote the article "Autistic Disturbances of

Angelman Syndrome and Prader-Willi Syndrome Essay
Angelman Syndrome & Prader–Willi Syndrome
Introduction
Prader–Willi and Angelman Syndrome are two genetic disorders with vastly differing phenotypes
linked by missing genetic imprints on the 15th chromosome's q arm between regions 11 and 13 .
While both orders result in mental deficits, their symptoms are otherwise segregated from the other
in their entirety. The differences in the disorders are the result of differing DNA methylation patterns
present in maternally and paternally inherited DNA. If the deletion occurs in the mother's DNA,
then Prader–Willi Syndrome appears. When the deletion occurs in the father's DNA, Angelman
Syndrome is the result.
The phenotypical differences between the two disorders are drastic. Those with ... Show more
content on Helpwriting.net ...
The Nature of the Disease Angelman syndrome is thought to be caused mainly by the deletion of the
maternally inherited copy of UEB3A. A small number of cases are also caused by failures in
imprinting or, very rarely, monosomy 15 in the egg and disomy 15 in the sperm. The profound
mental effects are caused by this gene due to the fact that, while UEB3A's protein is active in
various bodily tissues, only the mother's copy of the gene is active in the brain. The phenotype of
Angelman Syndrome is not overt enough to be detected unless it is being specifically looked for.
EEG scans are capable of detecting the disease at early ages, before it is otherwise possible to
detect.
Prader–Willi
Prader–Willi is caused by either deletions, failure in imprinting, or monosomy/disomy 15 from the
father's side. The genes involved are known to include, but are not known to be limited to SNRPN
and NDN. NDN odes for the protein Necdin, which, in rodents, interacts with neurotrophin
receptors in a way that is not completely understood to promote normal cognitive development.
SNRPN codes for several products, including small nucleolar RNAs, a splicing factor involved in
RNA processing, and a polypeptide known as SNURF. The precise role of this gene is unknown.
Symptoms. Prader–Willi syndrome presents symptoms beginning in utero, where the fetus is less
active than one without the

The Autobiography Look Me The Eye By John Elder Robison
Courage George Carlin, an American stand–up comedian and author, once said, "I like it when a
flower or a little tuft of grass grows through a crack in the concrete. It 's so f****n ' heroic." The
autobiography Look Me in the Eye by John Elder Robison is a memoir about a man's strange
aloofness towards others, but also the difficulties he has had to over–come and the courage he
needed to get through them. This story gives a glimpse into the life of an Aspergergian– as he likes
to call himself. Aspergers syndrome is a form of autism that affects the ability to effectively
socialize and communicate. This syndrome generated a vast majority of complications all
throughout his life. During his childhood, John is a social outcast. He does not know how to
befriend people, and he is very blunt and rude to his peers. This makes it very difficult for him to
create bonds with people, but he did occasionally become acquainted with the other outcasts such as
his friend named Jeff. Robinson's teenage years were even worse. John was labeled as the "class–
clown" and began to fail school even though he was very smart he just did not care anymore;
consequently, this lead him into the path of dropping out of school. However, after he quit school he
had started working for a small band fixing their EQ amps. This was good for John because it gave
him a chance to interact more with people while making money and traveling. After that, he started
working for successful bands like KISS and Pink

Gulf War Syndrome Essay
Gulf War Syndrome
The Gulf War Syndrome was identified after the Gulf War in 1991. Thousands of troops from the
US, British, and Canadian developed symptoms after the war. This Syndrome has been researched
since the end of the Gulf War and still not all the answers have been found. Not only have thousands
of troops suffered from this syndrome, but also their families have developed some symptoms
related to this syndrome. It is important to inform our nation of this new disease because there is still
no cure, and GWS can be our next conflict relating to AIDS and Cancer. This research is dedicated
to people who are uneducated about Gulf War Syndrome. After reading many articles about Gulf
War Syndrome there is still no ... Show more content on Helpwriting.net ...
Syndrome–2 or "Confusion–ataxia'; Syndrome – characterized by problems with thinking and
reasoning processes such as reading, writing, and spelling: getting confused; getting disoriented
when trying to locate a car in a parking lot; having problems with balance; having a physician's
diagnosis of post–traumatic stress disorder, depression, or liver disease; and sexual impotence ("
Gulf War Illnesses Broken Down Into Three Primary Syndromes'; 2).
Syndrome–3 or "Artho–myo–neuropathy'; Syndrome – characterized by generalized joint and
muscle pains, increased difficulty lifting heavy objects, fatigue, and tingling or numbness of the
hands, arms, feet, and legs (" Gulf War Illnesses Broken Down Into Three Primary Syndromes'; 1–
2). The Gulf War Syndrome has over 20 symptoms that have been reported by the veterans of the
Gulf War. According to Stephen Straus in the journal The Lancet, over 50,000 troops returned as
changed men. Reports showed of vascular instability, hyperventilation, bacilliuria, and other
physiological and laboratory anomalies in the Gulf War veterans. When the problem began to exist,
the US alone funded $ 115,000,000 for targeted research on the unknown syndrome. Four thousand
gulf war veterans and men who also served in Bosnia were mailed questionnaires about deployment,
exposures, symptoms, and illnesses. The main finding was that the Gulf War

Autism Spectrum Disorder Case Study
Through assessment, the child more often than not will be observed in the classroom as it is a
natural setting for the student. During this developmental age, interventions are focused towards the
child's success in the educational setting (Stoddart, 2005). It is important to find the right classroom
fit for each child as bullying is an issue that could come about from the child's characteristics that
come along with Asperger Syndrome (Stoddart, 2005). Eleven is the average age of diagnosis for
Asperger Syndrome. Although eleven is the average, many characteristics can be noticeable during
the infancy and early childhood years (Stoddart, 2005). Adolescence is considered from ages 12 to
18. During this developmental age, the individual ... Show more content on Helpwriting.net ...
The feeling of being left behind can cause a state of depression for these individuals (Stoddart,
2005). Services of treatment for mental health disorders start ending at the age of 18; it can difficult
transitioning to adult services for Asperger Syndrome. This can be a stressful time of getting
treatment for both the individual and supporters of the individual. This proves that it is better for the
diagnosis to be earlier rather than later so there is more time while the help is more widely available
before the individual turns 18 years old (Stoddart, 2005).
Middle Adulthood comes next consisting from age 31 to 50. Because of social defects, typical tasks
such as increasing independence from family origin, dating and marriages, and procreation can be a
major struggle (Stoddart, 2005). There are a great amount of divorces that come from relationships
with one of the individuals having Asperger Syndrome or Autistic Spectrum Disorder. There are
individuals that make it this late in life without being diagnosed with either disease and at this point
if at this point they are diagnosed the individual, and or the individual's supporters are ecstatic to
have

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