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Related to neurofibromatosis: Neurofibromatosis Type 2, Neurofibromatosis Type 1
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org), neurofibromatosis is a genetic disorder that occurs in one of every 3,000 people worldwide.
Neurofibromatosis Type 1 (NF1) causes nerve tissues to grow into tumor and bone deformity.
7] Based on our literature review, 10 previous reports of solitary benign intrascrotal extratesticular schwannomas unassociated with neurofibromatosis or schwannomatosis involved patients ages between 24 and 71.
Major Finding: A database review found that pregnant women with neurofibromatosis type 1 were more likely to develop preeclampsia (OR, 2.
As healthcare professionals providing primary eye care for a large population, optometrists may encounter patients with NF and therefore should recognize the first signs of this disease, and also should be aware of the ocular implications of the neurofibromatosis diseases, so that appropriate remedial action can be sought through referral to a specialist.
Neurofibromatosis type 1 (previously known as von Recklinghausen disease) is an autosomal dominant disorder affecting roughly 1 in 3000 persons and is characterized by the mutation of the neurofibromin gene on chromosome 17q11.
Last September Archie was officially diagnosed with Neurofibromatosis Type 1.
Occur in 5% of individuals affected with neurofibromatosis type 1
The new experiments have estimated that the incidence of neurofibromatosis type 2 may be as high as 1 in 25,000 people.
8 In the present case, no neurofibroma was found anterior to C2, and since it is a widely accepted fact that in neurofibromatosis there is genetically related maldevelopment of neuroectoderm and mesoderm, there may be associated deformities in the adjacent structures and ligaments--in turn leading to AAD.
The annual fundraising event asks celebrities to draw a doodle to raise money for two neurological charities, Epilepsy Action and The Neurofibromatosis Association.