Guidelines of care for neurofibromatosis type 1
โ Scribed by Lawrence F. Eichenfield; Moise L. Levy; Amy S. Paller; Vincent M. Riccardi; the Guidelines/Outcomes Committee*
- Book ID
- 117395786
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 452 KB
- Volume
- 37
- Category
- Article
- ISSN
- 1097-6787
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๐ SIMILAR VOLUMES
The prevalence of neurofibromatosis type 1 (NF1) is about 1/3,000. There are no known ethnic groups in which NF1 does not occur or is unusually common. The prevalence is somewhat higher in young children than in adults, a difference that probably results at least in part from the early death of some
Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder characterized by abnormalities of tissues predominantly derived from the neural crest. Symptoms are highly variable and severity cannot be predicted, even within families. DNA of 84 unrelated patients with NF1, unselected for clinical