Therapeutics for Childhood Neurofibromatosis Type 1 and Type 2
β Scribed by Simone L. Ardern-Holmes; Kathryn N. North
- Book ID
- 107559124
- Publisher
- Springer
- Year
- 2011
- Tongue
- English
- Weight
- 180 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1092-8480
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π SIMILAR VOLUMES
Neurofibromatosis 1 (NF1) is an autosomal dominant neurocutaneous disorder with an incidence of approximately 1 in 4000. Cognitive deficits and academic learning difficulties are the most common neurological 'complication' of NF1 in childhood and can be responsible for significant lifetime morbidity
Neurofibromatosis '&pe 1 (NF-1) is an autosomal dominant condition which has markedly variable clinical expression, with manifestations ranging from mild cutaneous lesions to severe orthopedic complications and functional impairment. The current obstetrical literature indicates that women with NF-1