Neurofibromatosis bul
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Neurofibromatosis Type 1
Neurofibromatosis Type 1 (NF1) is a genetic disorder caused by a mutation on chromosome 17 that results in benign tumors forming along nerves. It is characterized by multiple café-au-lait spots and benign tumors called neurofibromas that can form on or under the skin or in other tissues. NF1 has variable symptoms that can include bone abnormalities, learning disabilities, tumors in the brain or optic pathway that can impact vision, and high blood pressure. While there is no cure for NF1, symptoms can be treated through surgery, medication, physical therapy or genetic counseling.
Neurofibromatosis Social Media Trends -- a Medicine 2.0 Presentation
Inspire CEO Brian Loew discusses findings from Neurofibromatosis Social Media Trends, a survey report from the Inspire/Neurofibromatosis Network Support Community.
Presentation project
The document summarizes information about Neurofibromatosis (NF), a genetic disorder that causes tumors to grow on nerve endings. It describes the three main types of NF - NF1, NF2, and Schwannomatosis. It also outlines the mission of the Children's Tumor Foundation to support research, treatments, and patients affected by NF through funding, information resources, and advocacy efforts. Specific cases of individuals living with NF symptoms are provided. The document encourages supporting the Foundation's work to find cures and end NF.
NEUROFIBROMATOSIS TYPE I /prosthodontic courses
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.
Neurofibromatosis Social Media Trends February 2013
The document summarizes key findings from a study on neurofibromatosis patients' and caregivers' use of social media:
- Over 160 patients and 57 caregivers participated in the online survey. Most patients used social media to find information from others about managing their condition, while caregivers used it to support the person they care for.
- Patients with more severe forms of neurofibromatosis were more likely to view online communities as an essential resource and to seek differing opinions on treatments. Older patients and caregivers tended to be more regular and long-term users.
- Search engines, general health sites, and patient advocacy sites were the most common sources of information about neurofibrom
Cognitive Impairment In Children With Type 1 Neurofibromatosis
The document summarizes research on cognitive impairment in children with Type 1 Neurofibromatosis (NF1). It finds that 40-60% of children with NF1 experience cognitive disabilities such as lower IQ and poor academic achievement. While studies have identified structural brain abnormalities and specific learning disabilities in children with NF1, more research is still needed. In particular, a standardized diagnostic criteria and early assessment methods could help identify deficits earlier to improve intervention. Longitudinal studies are also recommended to determine how to best support children with NF1 and their families.
Neurofibromatosis
Neurofibromatosis (NF) is a genetic disorder that causes tumors to form on nerve tissues. There are two main types, NF1 and NF2. Symptoms can include café au lait spots, learning disabilities, bone deformities, pain, numbness, and trouble sleeping. NF is caused by mutations on chromosomes 17 and 22 that result in uncontrolled cell growth. It is usually diagnosed during a physical exam and may require eye, ear, imaging and genetic testing. Treatments include surgery, medication to manage symptoms, and lifelong monitoring due to risks of neurological problems, cancer and other complications. Support groups like the Children's Tumor Foundation provide resources for patients and their families.
Recommended
Neurofibromatosis Type 1
Neurofibromatosis Type 1 (NF1) is a genetic disorder caused by a mutation on chromosome 17 that results in benign tumors forming along nerves. It is characterized by multiple café-au-lait spots and benign tumors called neurofibromas that can form on or under the skin or in other tissues. NF1 has variable symptoms that can include bone abnormalities, learning disabilities, tumors in the brain or optic pathway that can impact vision, and high blood pressure. While there is no cure for NF1, symptoms can be treated through surgery, medication, physical therapy or genetic counseling.
Neurofibromatosis Social Media Trends -- a Medicine 2.0 Presentation
Inspire CEO Brian Loew discusses findings from Neurofibromatosis Social Media Trends, a survey report from the Inspire/Neurofibromatosis Network Support Community.
Presentation project
The document summarizes information about Neurofibromatosis (NF), a genetic disorder that causes tumors to grow on nerve endings. It describes the three main types of NF - NF1, NF2, and Schwannomatosis. It also outlines the mission of the Children's Tumor Foundation to support research, treatments, and patients affected by NF through funding, information resources, and advocacy efforts. Specific cases of individuals living with NF symptoms are provided. The document encourages supporting the Foundation's work to find cures and end NF.
NEUROFIBROMATOSIS TYPE I /prosthodontic courses
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.
Neurofibromatosis Social Media Trends February 2013
The document summarizes key findings from a study on neurofibromatosis patients' and caregivers' use of social media:
- Over 160 patients and 57 caregivers participated in the online survey. Most patients used social media to find information from others about managing their condition, while caregivers used it to support the person they care for.
- Patients with more severe forms of neurofibromatosis were more likely to view online communities as an essential resource and to seek differing opinions on treatments. Older patients and caregivers tended to be more regular and long-term users.
- Search engines, general health sites, and patient advocacy sites were the most common sources of information about neurofibrom
Cognitive Impairment In Children With Type 1 Neurofibromatosis
The document summarizes research on cognitive impairment in children with Type 1 Neurofibromatosis (NF1). It finds that 40-60% of children with NF1 experience cognitive disabilities such as lower IQ and poor academic achievement. While studies have identified structural brain abnormalities and specific learning disabilities in children with NF1, more research is still needed. In particular, a standardized diagnostic criteria and early assessment methods could help identify deficits earlier to improve intervention. Longitudinal studies are also recommended to determine how to best support children with NF1 and their families.
Neurofibromatosis
Neurofibromatosis (NF) is a genetic disorder that causes tumors to form on nerve tissues. There are two main types, NF1 and NF2. Symptoms can include café au lait spots, learning disabilities, bone deformities, pain, numbness, and trouble sleeping. NF is caused by mutations on chromosomes 17 and 22 that result in uncontrolled cell growth. It is usually diagnosed during a physical exam and may require eye, ear, imaging and genetic testing. Treatments include surgery, medication to manage symptoms, and lifelong monitoring due to risks of neurological problems, cancer and other complications. Support groups like the Children's Tumor Foundation provide resources for patients and their families.
Neurofibromatosis
The document discusses Whitney Roberts' mission to raise awareness of Neurofibromatosis Type 2 (NF2) through organizing a walk. NF2 is a rare genetic disorder that causes tumors on the cranial and spinal nerves. It affects about 1 in 40,000 people and can cause hearing loss, balance issues, and vision problems. Whitney plans to hold a walk similar to Relay for Life to educate people about NF2 and raise money for research, with the goal of increasing understanding of this little-known disorder.
Congenital glaucoma and neurofibromatosis type 1
case report of a 6 month old male child with congenital glaucoma associated with neurofibromatosis type 1
Neurofibromatosis
It is a brief description of the Neurofibromatosis genetic disorder.
The content include:
*Definition of Neurofibromatosis
*Symptoms of Neurofibromatosis
*Causes & Risk factors
*Complications
*Tests and diagnosis
*Treatments
References:
Robbins Basic Pathology, 9th Edition.
Medical Genetics, 4th Edition.
Myoclinic.
Neurofibromatosis abhijeet
Neurofibromatosis is a genetically inherited disorder that causes tumors to grow on nerve tissues. There are three main types: NF1 is the most common, caused by a mutation on chromosome 17 and characterized by cafe au lait spots and benign nerve tumors; NF2 results from a mutation on chromosome 22 and causes bilateral tumors of the vestibular nerve; schwannomatosis involves mutations on chromosomes 17 and 22 and causes tumors on cranial, spinal and peripheral nerves without hearing loss. Symptoms vary but can include discolored skin patches, nerve tumors, headaches, hearing loss, and in rare cases cancer. Diagnosis is based on clinical criteria and treatment focuses on managing symptoms through surgery or chemotherapy.
Neurofibromatosis
La neurofibromatosis es un trastorno genético dominante que causa tumores en los nervios periféricos y la piel. Existen dos tipos principales, el tipo 1 se debe a mutaciones en el gen NF1 y representa alrededor del 96% de los casos. Sus síntomas incluyen manchas café con leche en la piel, neurofibromas y nódulos de Lisch en el iris. No tiene cura pero el tratamiento incluye cirugía para remover tumores dolorosos o que causan otras complicaciones.
Neurofibromatosis
Neurofibromatosis (NF) is a genetic disorder that causes tumors to form in the nervous system. There are two main types, NF1 and NF2. NF1 is caused by a mutation on chromosome 17 and affects nerve cell growth, while NF2 is caused by a mutation on chromosome 22 and affects tumor suppression. The main symptoms and characteristics of each type are described. Both types are inherited in an autosomal dominant pattern and can be passed down through families. There is no cure for NF, and treatment focuses on surgically removing tumors when possible.
Convivir con neurofibromatosis.
Las nuerofibromatosis son un grupo de enfermedades de origen genético que afectan principalmente al desarrollo y crecimiento de los tejidos de las células nerviosas.
Congenital pseudoarthrosis
1. Congenital pseudoarthrosis of the tibia (CPT) is a rare congenital defect involving non-union of the tibia.
2. It is classified into six types by Boyd based on location and characteristics of the defect.
3. Types 1-4 involve the tibia, while types 5-6 may also involve the fibula or other sites. Common features include anterolateral bowing of the tibia and pseudarthrosis formation.
How to Thrive: A Redefinition of Success
As more and more people are coming to realize, there is far more to living a truly successful life than just earning a bigger salary and capturing a corner office. Our relentless pursuit of the two traditional metrics of success - money and power - has led to an epidemic of burnout and stress-related illnesses, and an erosion in the quality of our relationships, family life, and, ironically, our careers. In being connected to the world 24/7, we're losing our connection to what truly matters.
Drawing on the latest groundbreaking research and scientific findings in the fields of psychology, sports, sleep, and physiology that show the profound and transformative effects of meditation, mindfulness, unplugging, and giving, I show us the way to a revolution in our culture, our thinking, our workplace, and our lives.
This presentation is a visual excerpt of my book, Thrive. To read more, go to: http://thrive.huffingtonpost.com/
The 10 Best Copywriting Formulas for Social Media Headlines
A Top Ten list of the best copywriting formulas used by writers and marketers, and how they might fit with the social media headlines you write.
1. Before – After – Bridge
2. Problem – Agitate – Solve
3. Features – Advantages – Benefits (FAB)
4. The 4 C’s
5. The 4 U’s
6. Attention – Interest – Desire – Action (AIDA)
7. A FOREST
8. The 5 basic objections
9. Picture – Promise – Prove – Push (PPPP)
10. The 1 – 2 – 3 – 4 Formula for Persuasive Copy
The complete list is available on the Buffer blog here: https://blog.bufferapp.com/copywriting-formulas
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Neurofibromatosis
The document discusses Whitney Roberts' mission to raise awareness of Neurofibromatosis Type 2 (NF2) through organizing a walk. NF2 is a rare genetic disorder that causes tumors on the cranial and spinal nerves. It affects about 1 in 40,000 people and can cause hearing loss, balance issues, and vision problems. Whitney plans to hold a walk similar to Relay for Life to educate people about NF2 and raise money for research, with the goal of increasing understanding of this little-known disorder.
Congenital glaucoma and neurofibromatosis type 1
case report of a 6 month old male child with congenital glaucoma associated with neurofibromatosis type 1
Neurofibromatosis
It is a brief description of the Neurofibromatosis genetic disorder.
The content include:
*Definition of Neurofibromatosis
*Symptoms of Neurofibromatosis
*Causes & Risk factors
*Complications
*Tests and diagnosis
*Treatments
References:
Robbins Basic Pathology, 9th Edition.
Medical Genetics, 4th Edition.
Myoclinic.
Neurofibromatosis abhijeet
Neurofibromatosis is a genetically inherited disorder that causes tumors to grow on nerve tissues. There are three main types: NF1 is the most common, caused by a mutation on chromosome 17 and characterized by cafe au lait spots and benign nerve tumors; NF2 results from a mutation on chromosome 22 and causes bilateral tumors of the vestibular nerve; schwannomatosis involves mutations on chromosomes 17 and 22 and causes tumors on cranial, spinal and peripheral nerves without hearing loss. Symptoms vary but can include discolored skin patches, nerve tumors, headaches, hearing loss, and in rare cases cancer. Diagnosis is based on clinical criteria and treatment focuses on managing symptoms through surgery or chemotherapy.
Neurofibromatosis
La neurofibromatosis es un trastorno genético dominante que causa tumores en los nervios periféricos y la piel. Existen dos tipos principales, el tipo 1 se debe a mutaciones en el gen NF1 y representa alrededor del 96% de los casos. Sus síntomas incluyen manchas café con leche en la piel, neurofibromas y nódulos de Lisch en el iris. No tiene cura pero el tratamiento incluye cirugía para remover tumores dolorosos o que causan otras complicaciones.
Neurofibromatosis
Neurofibromatosis (NF) is a genetic disorder that causes tumors to form in the nervous system. There are two main types, NF1 and NF2. NF1 is caused by a mutation on chromosome 17 and affects nerve cell growth, while NF2 is caused by a mutation on chromosome 22 and affects tumor suppression. The main symptoms and characteristics of each type are described. Both types are inherited in an autosomal dominant pattern and can be passed down through families. There is no cure for NF, and treatment focuses on surgically removing tumors when possible.
Convivir con neurofibromatosis.
Las nuerofibromatosis son un grupo de enfermedades de origen genético que afectan principalmente al desarrollo y crecimiento de los tejidos de las células nerviosas.
Congenital pseudoarthrosis
1. Congenital pseudoarthrosis of the tibia (CPT) is a rare congenital defect involving non-union of the tibia.
2. It is classified into six types by Boyd based on location and characteristics of the defect.
3. Types 1-4 involve the tibia, while types 5-6 may also involve the fibula or other sites. Common features include anterolateral bowing of the tibia and pseudarthrosis formation.
How to Thrive: A Redefinition of Success
As more and more people are coming to realize, there is far more to living a truly successful life than just earning a bigger salary and capturing a corner office. Our relentless pursuit of the two traditional metrics of success - money and power - has led to an epidemic of burnout and stress-related illnesses, and an erosion in the quality of our relationships, family life, and, ironically, our careers. In being connected to the world 24/7, we're losing our connection to what truly matters.
Drawing on the latest groundbreaking research and scientific findings in the fields of psychology, sports, sleep, and physiology that show the profound and transformative effects of meditation, mindfulness, unplugging, and giving, I show us the way to a revolution in our culture, our thinking, our workplace, and our lives.
This presentation is a visual excerpt of my book, Thrive. To read more, go to: http://thrive.huffingtonpost.com/
The 10 Best Copywriting Formulas for Social Media Headlines
A Top Ten list of the best copywriting formulas used by writers and marketers, and how they might fit with the social media headlines you write.
1. Before – After – Bridge
2. Problem – Agitate – Solve
3. Features – Advantages – Benefits (FAB)
4. The 4 C’s
5. The 4 U’s
6. Attention – Interest – Desire – Action (AIDA)
7. A FOREST
8. The 5 basic objections
9. Picture – Promise – Prove – Push (PPPP)
10. The 1 – 2 – 3 – 4 Formula for Persuasive Copy
The complete list is available on the Buffer blog here: https://blog.bufferapp.com/copywriting-formulas
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The 10 Best Copywriting Formulas for Social Media Headlines
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