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Neurofibromatosis 2
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Neurofibromatosis 2 Learning Center
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Autosomal dominant hereditary disorder
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Neurofibromatosis 2
Neurofibromatosis 2(NF2) is a genetic disorder in which tumors form on the nerves of the brain and spine(the central nervous system).NF2; Bilateral acoustic neurofibromatosis; Central bilateral acoustic NF.NF2 is passed...
Basic Info
Symptoms
Symptoms of NF2 include:Balance problemsCataracts at a young ageChanges in visionCoffee-colored marks on the skinFaci...
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Causes
NF2 is passed down through families in an autosomal dominant fashion. This means that if one parent has NF2, any chi...
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Tests
Signs include:Brain and spinal tumorsHearing-related (acoustic) tumorsSkin tumorsTests include:Genetic testingMedical...
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Treatments
Most patients need surgery to remove tumors. Tumors also can be treated with radiation.
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Available Treatments
Drugs
No Known Drug Therapy
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Risk Factors
family history of Neurofibromatosis 2
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Complications
Brain Tumors
Deafness
Cataract
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Prevention
Genetic Counseling
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Doctor Specialties
Neurologist
Oncologist
Pediatrician
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Basic Info
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Primary pediatric intraspinal sarc...
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Honoring Jessica
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Neurofibromatosis 2
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Related Topics
Autosomal dominant hereditary disorder
Acute Intermittent Porphyria
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,
Basal Cell Nevus Syndrome
,
Branchio-Oto-Renal Syndrome
,
Cleidocranial Dysplasia
,
Hereditary Angioedema
,
hereditary nephrogenic diabetes insipidus
,
LEOPARD Syndrome
,
Marfan's Syndrome
,
Multiple Hereditary Exostoses
,
Myotonia Congenita
,
Neurofibromatosis 2
,
Noonan Syndrome
,
Peutz-Jeghers Syndrome
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