Anorexia nervoasa
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Anorexia most commonly has its onset during adolescence, especially among girls aged 9 to 12, though it can affect people of any age, gender, race or background. Anorexia nervosa occurs 10 times more frequently in females than males. Anorexia is associated with depression, obsession with dieting and weight loss, hair loss, and unhealthy weight loss methods like diet pills, laxatives and vomiting.
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Down Syndrome Child
The document provides an overview of Down syndrome, including its history, types, physical characteristics, diagnosis, informing parents, and caring for an affected child. It discusses John Langdon Down's initial description in 1866 and the recognition as a genetic disorder in 1959. It covers the three types of trisomy 21, translocation, and mosaicism. Key physical signs include a flat face, slanted eyes, small ears and hands/feet. Parents should be informed clearly using understandable language and focusing on positive aspects while avoiding strict prognosis. Acceptance, stimulation, social integration and support are important for caring for a child with Down syndrome.
Down syndrome - Child Health Nursing, M.Sc(N)
Down syndrome is a genetic condition caused by the presence of an extra chromosome 21. It causes delays in physical and intellectual development. The majority of cases are caused by nondisjunction during cell division resulting in 47 total chromosomes rather than the usual 46. Clinical manifestations include mild to moderate intellectual disability, delayed development, congenital heart defects, vision and hearing problems, and increased risk of infections. Nursing care focuses on monitoring for complications, promoting development, and educating families on managing care.
Down syndrome
Down syndrome is a chromosomal condition caused by the presence of an extra copy of chromosome 21. It is often associated with delays in cognitive ability and physical growth. Individuals with Down syndrome typically have an IQ around 50, compared to 100 for those without it, and many have severe intellectual disabilities.
Down syndrome
This document discusses Down syndrome, including its causes, features in newborns, diagnosis, and management. Down syndrome results from extra genetic material from chromosome 21, which can occur through trisomy 21, mosaicism, or translocation. Affected newborns commonly have hypotonia, slanted eyes, and other physical signs. Prenatal screening and testing can detect Down syndrome. Early intervention aims to support development and address any health issues.
Down syndrome Class Presentation
Down Syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of a third copy of chromosome 21. It is the most common chromosome abnormality in humans, occurring in about 1 in 699 births in the US. Down Syndrome can be broken into three main types - trisomy 21 which accounts for 95% of cases, translocation Down Syndrome which is 3-4% of cases, and mosaic Down Syndrome which is less than 1% of cases. Physical features include stunted growth, slanted eyes, low-set ears, flattened nose, smaller teeth and shortened hands. Individuals with Down Syndrome often have intellectual disabilities ranging from mild to moderate and may experience delays in speech, motor skills,
Down Syndrome
Down syndrome is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. It was first described in 1866 by Dr. John Langdon Down and the chromosome abnormality was discovered in 1959. Individuals with Down syndrome typically have physical and intellectual disabilities including an average IQ of 50, equivalent to an 8 or 9 year old child. They also have an increased risk of health problems such as congenital heart disease and leukemia. Life expectancy for individuals with Down syndrome has increased from 12 years in 1912 to 50-60 years currently with improved medical care.
down syndrome-
This document provides information about Down syndrome including:
- Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It was first described in 1866 and identified as a chromosome abnormality in 1959.
- Individuals with Down syndrome often have cognitive disabilities and characteristic physical traits such as a flat nasal bridge, upward slanting eyes, and small mouth. They also have an increased risk of health issues like heart defects and hearing loss.
- Down syndrome is usually caused by a chromosomal abnormality called trisomy 21, but can also be due to mosaicism or translocations. The risk increases with older parental age and a family history of Down syndrome. Prognosis has improved with
What is down syndrome
Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It is characterized by intellectual disability and developmental delays, a distinct facial appearance, and weak muscle tone. There are three main types - trisomy 21, translocation, and mosaicism. While people with Down syndrome experience cognitive delays, the intellectual disability is usually mild to moderate. With proper support and care, people with Down syndrome can learn skills, go to school, work, and live independently or within a supportive community.
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Down Syndrome Child
The document provides an overview of Down syndrome, including its history, types, physical characteristics, diagnosis, informing parents, and caring for an affected child. It discusses John Langdon Down's initial description in 1866 and the recognition as a genetic disorder in 1959. It covers the three types of trisomy 21, translocation, and mosaicism. Key physical signs include a flat face, slanted eyes, small ears and hands/feet. Parents should be informed clearly using understandable language and focusing on positive aspects while avoiding strict prognosis. Acceptance, stimulation, social integration and support are important for caring for a child with Down syndrome.
Down syndrome - Child Health Nursing, M.Sc(N)
Down syndrome is a genetic condition caused by the presence of an extra chromosome 21. It causes delays in physical and intellectual development. The majority of cases are caused by nondisjunction during cell division resulting in 47 total chromosomes rather than the usual 46. Clinical manifestations include mild to moderate intellectual disability, delayed development, congenital heart defects, vision and hearing problems, and increased risk of infections. Nursing care focuses on monitoring for complications, promoting development, and educating families on managing care.
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Down syndrome is a chromosomal condition caused by the presence of an extra copy of chromosome 21. It is often associated with delays in cognitive ability and physical growth. Individuals with Down syndrome typically have an IQ around 50, compared to 100 for those without it, and many have severe intellectual disabilities.
Down syndrome
This document discusses Down syndrome, including its causes, features in newborns, diagnosis, and management. Down syndrome results from extra genetic material from chromosome 21, which can occur through trisomy 21, mosaicism, or translocation. Affected newborns commonly have hypotonia, slanted eyes, and other physical signs. Prenatal screening and testing can detect Down syndrome. Early intervention aims to support development and address any health issues.
Down syndrome Class Presentation
Down Syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of a third copy of chromosome 21. It is the most common chromosome abnormality in humans, occurring in about 1 in 699 births in the US. Down Syndrome can be broken into three main types - trisomy 21 which accounts for 95% of cases, translocation Down Syndrome which is 3-4% of cases, and mosaic Down Syndrome which is less than 1% of cases. Physical features include stunted growth, slanted eyes, low-set ears, flattened nose, smaller teeth and shortened hands. Individuals with Down Syndrome often have intellectual disabilities ranging from mild to moderate and may experience delays in speech, motor skills,
Down Syndrome
Down syndrome is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. It was first described in 1866 by Dr. John Langdon Down and the chromosome abnormality was discovered in 1959. Individuals with Down syndrome typically have physical and intellectual disabilities including an average IQ of 50, equivalent to an 8 or 9 year old child. They also have an increased risk of health problems such as congenital heart disease and leukemia. Life expectancy for individuals with Down syndrome has increased from 12 years in 1912 to 50-60 years currently with improved medical care.
down syndrome-
This document provides information about Down syndrome including:
- Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It was first described in 1866 and identified as a chromosome abnormality in 1959.
- Individuals with Down syndrome often have cognitive disabilities and characteristic physical traits such as a flat nasal bridge, upward slanting eyes, and small mouth. They also have an increased risk of health issues like heart defects and hearing loss.
- Down syndrome is usually caused by a chromosomal abnormality called trisomy 21, but can also be due to mosaicism or translocations. The risk increases with older parental age and a family history of Down syndrome. Prognosis has improved with
What is down syndrome
Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It is characterized by intellectual disability and developmental delays, a distinct facial appearance, and weak muscle tone. There are three main types - trisomy 21, translocation, and mosaicism. While people with Down syndrome experience cognitive delays, the intellectual disability is usually mild to moderate. With proper support and care, people with Down syndrome can learn skills, go to school, work, and live independently or within a supportive community.
Down syndrome
Pediatrics. trisomy 21. Meiotic non-disjunction of chromosome 21. clinical features and associated abnormalities of down syndrome. screening test for down syndrome. counseling for parents in down syndrome.
Down Syndrome 1
Down syndrome, also known as trisomy 21, is a genetic disorder caused by a third copy of chromosome 21. It is associated with physical growth delays and distinctive facial features. People with Down syndrome typically have mild to moderate intellectual disabilities, with an average IQ of around 50. While Down syndrome is not caused by environmental factors or a parent's genetics, it can be identified during pregnancy through screening and testing. Individuals with Down syndrome often require regular health checks as they are at greater risk for health problems and have reduced life expectancy compared to the general population.
Down Syndrome
Down Syndrome is caused by the presence of an extra chromosome 21 or part of an extra chromosome 21. It is also known as Trisomy 21. Common symptoms include a round face, broad head, excess joint laxity, and an IQ range of 10-70. The incidence rates are 1 per 800 to 1 per 1000 births depending on the mother's age, with older mothers having higher risks. While there is no prevention or cure, testing like amniocentesis can detect Down Syndrome during pregnancy. Support organizations like the National Down Syndrome Society provide help for children with Down Syndrome.
Down syndrome
Down syndrome is a genetic condition where a person has three copies of chromosome 21 instead of the usual two. This extra genetic material causes developmental delays and other issues. Down syndrome can range from mild to severe depending on the individual. Over 90% of Down syndrome cases are caused by trisomy 21, where there are three copies of chromosome 21. Physical signs include a flattened nose, small ears and mouth, upward slanting eyes, and short hands and fingers. The risk of having a child with Down syndrome increases with the mother's age. Complications can include heart defects, leukemia, and early-onset Alzheimer's disease.
Down Syndrome
Down syndrome is a genetic condition where a person has three copies of chromosome 21 instead of the usual two. This extra genetic material causes developmental delays and other issues. Down syndrome can range from mild to severe depending on the individual. The majority of Down syndrome cases are not inherited and are caused by random errors during cell division. Common physical signs include a flattened face, small ears and mouth, upward slanting eyes, and decreased muscle tone at birth. The risk of having a child with Down syndrome increases with the mother's age. Screening tests during pregnancy can detect 87% of Down syndrome cases. Diagnostic tests like amniocentesis or CVS can confirm a Down syndrome diagnosis. Individuals with Down syndrome may experience health
Down syndrome awareness
Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It is characterized by cognitive delays, slower physical development, and distinctive facial features. Individuals with Down syndrome often have health issues such as heart defects, hearing or vision problems, thyroid issues, and an increased risk of Alzheimer's disease. Their development follows a specific pattern, with relative strengths in social skills but delays in motor skills, language, and short-term verbal memory. Early intervention and education can help maximize their learning potential over their lifetime.
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Down's Syndrome, also known as trisomy 21, is a genetic condition where a person has 47 chromosomes instead of the usual 46, causing mental retardation and other problems ranging from mild to serious. Common physical signs include a flattened nose, small ears and mouth, upward slanting eyes, and short hands and fingers. Risk factors include increased maternal age and parents being carriers of the translocation. While there is no cure, early intervention and treatment of complications like heart defects can help development.
Care of Pediatric Down Syndrome
Down Syndrome is the most common chromosomal abnormality affecting children today. It occurs in approximately 1 in 800 to 1,000 births and is caused by the presence of an extra copy of chromosome 21. Individuals with Down Syndrome often have intellectual disabilities and are at increased risk for certain medical conditions such as congenital heart disease, gastrointestinal abnormalities, hearing loss, thyroid disorders, and periodontal disease. Proper screening, monitoring, and management of associated health issues can help improve quality of life for those with Down Syndrome.
Down Syndrome
Down syndrome is a genetic condition where a person is born with an extra chromosome 21. It occurs in 1 in 800 live births. There are three types of Down syndrome - trisomy 21, mosaicism, and translocation. Trisomy 21 is the most common type, affecting 95% of people with Down syndrome. People with Down syndrome may experience some physical and developmental differences but should not be defined by their syndrome. With support, people with Down syndrome can lead fulfilling lives.
Down syndrome
Down syndrome is a genetic disorder caused by a full or partial extra copy of chromosome 21. This additional genetic material alters development and causes characteristic physical traits like low muscle tone, small stature, and a single deep crease in the palm. Early intervention through therapies can help children with Down syndrome achieve basic skills and lay a foundation for future progress, as delays are common in areas like physical, cognitive, language, and social development. Education requires careful consideration and supports, though with interventions people with Down syndrome can learn at their own pace and have varied goals and roles.
Down syndrome
Down syndrome is a genetic disorder caused by the presence of an extra copy of chromosome 21. It is associated with physical growth delays, distinctive facial features, and mild to moderate intellectual disabilities. The average IQ of a young adult with Down syndrome is equivalent to an 8- or 9-year-old, but IQ levels vary widely. Common health issues for those with Down syndrome include congenital heart disease, thyroid problems, vision and hearing disorders, and susceptibility to leukemia. While individuals with Down syndrome have some intellectual disabilities, they should be treated with dignity and respect.
Down Syndrome
Down Syndrome occurs when there is an extra chromosome on the 21st chromosome. This leads to certain physical characteristics and health issues. While there is no cure, treatments can help address medical problems and therapy can help with skills. Research continues to seek a cure and help future patients.
down syndrome 2
The document discusses Down syndrome, which is caused by trisomy of chromosome 21 resulting in 47 total chromosomes instead of the typical 46. Individuals with Down syndrome have increased risk based on advanced maternal age and are more likely to have certain physical traits like a flat face and short hands. The condition was first described in 1866 and its genetic basis was discovered in 1930. Current research uses mouse models to study specific genes on chromosome 21 that may contribute to Down syndrome phenotypes.
Down Syndrome 2
Down syndrome is the most common cause of developmental disability in newborns, occurring due to the presence of an extra chromosome. It affects 1 in 800 live births and the risk increases with the age of the mother. Symptoms include a flat nose, small mouth, slanting eyes, as well as adverse effects on hearing and sight like frequent ear infections leading to hearing loss requiring aids. While there is no prevention or cure, screening and diagnostic tests can determine the risk and manage symptoms through regular checkups and medication. Support is available through organizations providing information, love, structure and community.
Down syndrome update 2014
Down Syndrome Update provides an overview of Down syndrome including its history, genetics, features, and recent research. It summarizes that Down syndrome is caused by trisomy 21 and describes the essential information that should be conveyed when delivering a diagnosis, such as the genetic basis, physical features, medical complications, intellectual disability, long-term prognosis, and support resources. Recent studies discussed include identifying the most important information for parents, social conditions of people with Down syndrome in Denmark, and the establishment of the US National Down Syndrome Registry called DS-Connect.
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This documentary explores mental health issues among teenagers by interviewing college students aged 17-18, an experienced psychologist, and an academic coach about their views on mental health challenges facing this age group. Statistics are provided on the prevalence of various mental health conditions in the UK population, such as depression, anxiety, phobias, and eating disorders. Close to 1 in 4 people are directly affected by a mental health issue.
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Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It is characterized by mild to moderate intellectual disability and distinctive facial features. The document discusses the history, genetics, clinical features, health issues, diagnosis and management of Down syndrome. Key points include that the risk increases with maternal age, common physical signs include a flat facial profile and hypotonia, associated conditions affect the heart, GI tract and thyroid, and treatment involves screening and early intervention.
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Pediatrics. trisomy 21. Meiotic non-disjunction of chromosome 21. clinical features and associated abnormalities of down syndrome. screening test for down syndrome. counseling for parents in down syndrome.
Down Syndrome 1
Down syndrome, also known as trisomy 21, is a genetic disorder caused by a third copy of chromosome 21. It is associated with physical growth delays and distinctive facial features. People with Down syndrome typically have mild to moderate intellectual disabilities, with an average IQ of around 50. While Down syndrome is not caused by environmental factors or a parent's genetics, it can be identified during pregnancy through screening and testing. Individuals with Down syndrome often require regular health checks as they are at greater risk for health problems and have reduced life expectancy compared to the general population.
Down Syndrome
Down Syndrome is caused by the presence of an extra chromosome 21 or part of an extra chromosome 21. It is also known as Trisomy 21. Common symptoms include a round face, broad head, excess joint laxity, and an IQ range of 10-70. The incidence rates are 1 per 800 to 1 per 1000 births depending on the mother's age, with older mothers having higher risks. While there is no prevention or cure, testing like amniocentesis can detect Down Syndrome during pregnancy. Support organizations like the National Down Syndrome Society provide help for children with Down Syndrome.
Down syndrome
Down syndrome is a genetic condition where a person has three copies of chromosome 21 instead of the usual two. This extra genetic material causes developmental delays and other issues. Down syndrome can range from mild to severe depending on the individual. Over 90% of Down syndrome cases are caused by trisomy 21, where there are three copies of chromosome 21. Physical signs include a flattened nose, small ears and mouth, upward slanting eyes, and short hands and fingers. The risk of having a child with Down syndrome increases with the mother's age. Complications can include heart defects, leukemia, and early-onset Alzheimer's disease.
Down Syndrome
Down syndrome is a genetic condition where a person has three copies of chromosome 21 instead of the usual two. This extra genetic material causes developmental delays and other issues. Down syndrome can range from mild to severe depending on the individual. The majority of Down syndrome cases are not inherited and are caused by random errors during cell division. Common physical signs include a flattened face, small ears and mouth, upward slanting eyes, and decreased muscle tone at birth. The risk of having a child with Down syndrome increases with the mother's age. Screening tests during pregnancy can detect 87% of Down syndrome cases. Diagnostic tests like amniocentesis or CVS can confirm a Down syndrome diagnosis. Individuals with Down syndrome may experience health
Down syndrome awareness
Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It is characterized by cognitive delays, slower physical development, and distinctive facial features. Individuals with Down syndrome often have health issues such as heart defects, hearing or vision problems, thyroid issues, and an increased risk of Alzheimer's disease. Their development follows a specific pattern, with relative strengths in social skills but delays in motor skills, language, and short-term verbal memory. Early intervention and education can help maximize their learning potential over their lifetime.
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Down's Syndrome, also known as trisomy 21, is a genetic condition where a person has 47 chromosomes instead of the usual 46, causing mental retardation and other problems ranging from mild to serious. Common physical signs include a flattened nose, small ears and mouth, upward slanting eyes, and short hands and fingers. Risk factors include increased maternal age and parents being carriers of the translocation. While there is no cure, early intervention and treatment of complications like heart defects can help development.
Care of Pediatric Down Syndrome
Down Syndrome is the most common chromosomal abnormality affecting children today. It occurs in approximately 1 in 800 to 1,000 births and is caused by the presence of an extra copy of chromosome 21. Individuals with Down Syndrome often have intellectual disabilities and are at increased risk for certain medical conditions such as congenital heart disease, gastrointestinal abnormalities, hearing loss, thyroid disorders, and periodontal disease. Proper screening, monitoring, and management of associated health issues can help improve quality of life for those with Down Syndrome.
Down Syndrome
Down syndrome is a genetic condition where a person is born with an extra chromosome 21. It occurs in 1 in 800 live births. There are three types of Down syndrome - trisomy 21, mosaicism, and translocation. Trisomy 21 is the most common type, affecting 95% of people with Down syndrome. People with Down syndrome may experience some physical and developmental differences but should not be defined by their syndrome. With support, people with Down syndrome can lead fulfilling lives.
Down syndrome
Down syndrome is a genetic disorder caused by a full or partial extra copy of chromosome 21. This additional genetic material alters development and causes characteristic physical traits like low muscle tone, small stature, and a single deep crease in the palm. Early intervention through therapies can help children with Down syndrome achieve basic skills and lay a foundation for future progress, as delays are common in areas like physical, cognitive, language, and social development. Education requires careful consideration and supports, though with interventions people with Down syndrome can learn at their own pace and have varied goals and roles.
Down syndrome
Down syndrome is a genetic disorder caused by the presence of an extra copy of chromosome 21. It is associated with physical growth delays, distinctive facial features, and mild to moderate intellectual disabilities. The average IQ of a young adult with Down syndrome is equivalent to an 8- or 9-year-old, but IQ levels vary widely. Common health issues for those with Down syndrome include congenital heart disease, thyroid problems, vision and hearing disorders, and susceptibility to leukemia. While individuals with Down syndrome have some intellectual disabilities, they should be treated with dignity and respect.
Down Syndrome
Down Syndrome occurs when there is an extra chromosome on the 21st chromosome. This leads to certain physical characteristics and health issues. While there is no cure, treatments can help address medical problems and therapy can help with skills. Research continues to seek a cure and help future patients.
down syndrome 2
The document discusses Down syndrome, which is caused by trisomy of chromosome 21 resulting in 47 total chromosomes instead of the typical 46. Individuals with Down syndrome have increased risk based on advanced maternal age and are more likely to have certain physical traits like a flat face and short hands. The condition was first described in 1866 and its genetic basis was discovered in 1930. Current research uses mouse models to study specific genes on chromosome 21 that may contribute to Down syndrome phenotypes.
Down Syndrome 2
Down syndrome is the most common cause of developmental disability in newborns, occurring due to the presence of an extra chromosome. It affects 1 in 800 live births and the risk increases with the age of the mother. Symptoms include a flat nose, small mouth, slanting eyes, as well as adverse effects on hearing and sight like frequent ear infections leading to hearing loss requiring aids. While there is no prevention or cure, screening and diagnostic tests can determine the risk and manage symptoms through regular checkups and medication. Support is available through organizations providing information, love, structure and community.
Down syndrome update 2014
Down Syndrome Update provides an overview of Down syndrome including its history, genetics, features, and recent research. It summarizes that Down syndrome is caused by trisomy 21 and describes the essential information that should be conveyed when delivering a diagnosis, such as the genetic basis, physical features, medical complications, intellectual disability, long-term prognosis, and support resources. Recent studies discussed include identifying the most important information for parents, social conditions of people with Down syndrome in Denmark, and the establishment of the US National Down Syndrome Registry called DS-Connect.
Documentary script
This documentary explores mental health issues among teenagers by interviewing college students aged 17-18, an experienced psychologist, and an academic coach about their views on mental health challenges facing this age group. Statistics are provided on the prevalence of various mental health conditions in the UK population, such as depression, anxiety, phobias, and eating disorders. Close to 1 in 4 people are directly affected by a mental health issue.
Down syndrome
Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It can be caused by trisomy 21, translocation, or mosaicism. Common symptoms include distinctive facial features, poor muscle tone, cognitive delays, and heart defects. While there is no cure, early intervention including speech, physical, and occupational therapy can help children with Down syndrome reach their full potential. Lifespan and quality of life have improved significantly in recent decades for those living with Down syndrome.
Down Syndrome
The document provides an overview of Down syndrome including definitions, features in newborns, common abnormalities, and age-specific healthcare guidelines. It notes that Down syndrome is caused by trisomy of chromosome 21 and occurs in approximately 1 in 660 births. Newborns with Down syndrome typically exhibit certain physical features such as slanted eyes and hypotonia. Common abnormalities include heart defects, gastrointestinal issues, hearing problems, and thyroid disorders. The document outlines guidelines for healthcare from the neonatal period through adulthood.
Down syndrome ppt for UGs
Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It is characterized by mild to moderate intellectual disability and distinctive facial features. The document discusses the history, genetics, clinical features, health issues, diagnosis and management of Down syndrome. Key points include that the risk increases with maternal age, common physical signs include a flat facial profile and hypotonia, associated conditions affect the heart, GI tract and thyroid, and treatment involves screening and early intervention.
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