Skip navigation
Results 1 - 10 of 63 for "Neurofibromatosis," type 2
  1. Genetics Home Reference: Neurofibromatosis type 2 From the National Institutes of Health (National Library of Medicine)  
    ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Neurofibromatosis type 2 On this page: Description Genetic changes Inheritance Diagnosis ...
  2. Neurofibromatosis Type 2: Information for Patients & Families by Mia MacCollin, M.D., Catherine Bove, R.N. Ed. & M. Priscilla ... professional providers' skills. Some frequently asked questions about Neurofibromatosis Type 2 Q. What are the chances of: a boy ...
  3. Neurocutaneous Syndromes (Nemours Foundation)  
    ... Therapy and specialists can help manage those symptoms. Neurofibromatosis Type 2 Neurofibromatosis type 2 is less common, occurring in about 1 in ...
  4. Neurofibromatosis (American Academy of Orthopaedic Surgeons)  
    ... is very difficult to treat and requires surgery. Neurofibromatosis Type 2 (NF2) Neurofibromatosis Type 2 is less common, occurring in 1 in 25,000 to 40,000 births. Also known as bilateral acoustic neurofibromatosis, NF2 mostly affects the central nervous system, causing ...
  5. ... Changes in the NF1 gene cause this disorder. Neurofibromatosis type 2: Less common than von Recklinghausen disease, this condition ... Changes in the NF2 gene are responsible for neurofibromatosis type 2. Tuberous sclerosis: Children with this condition may develop ...
  6. Neurofibromatosis 2 (NF2) is a genetic disorder in which tumors form on the nerves of the brain and ... Ferner RE. Neurofibromatosis 1 and neurofibromatosis 2: a twenty ... Neurocutaneous syndromes. In: Kliegman RM, Behrman RE, Jenson ...
  7. Neurofibromatosis (National Library of Medicine)  
    ... can become cancerous. There are three types of neurofibromatosis: Type 1 (NF1) causes skin changes and deformed bones. It usually starts in childhood. Sometimes the symptoms are present at birth. Type 2 (NF2) causes hearing loss, ringing in the ears, ...
  8. Neurofibromatosis From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... type 1 (NF1, also called von Recklinghaus disease), neurofibromatosis type 2 (NF2), and a type that was once considered to be a variation of NF2 but is now called schwannomatosis . An estimated ... NF1 is the most common neurofibromatosis, occurring in 1 in 3,000 to 4, ...
  9. Learning about Neurofibromatosis From the National Institutes of Health (National Human Genome Research Institute)  
    ... malignant tumors and may require treatment. Symptoms for neurofibromatosis type 2 include: Tumors along the eighth cranial nerve (schwannomas). ... for NF1 and NF2: GeneTests: Neurofibromatosis 1 GeneTests: Neurofibromatosis 2 Neurofibromatosis [marchofdimes.com] The March of Dimes funds ...
  10. Cancer Genetics Services Directory (National Cancer Institute)  
    ... Multiple myeloma, familial Neuroblastoma, hereditary Neurofibromatosis type 1 Neurofibromatosis type 2 Nijmegen breakage syndrome Pancreatic cancer, hereditary Paraganglioma, hereditary ...
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next