Neurofibromatosis type 1 and precocious puberty:Beyond the chasm
โ Scribed by Reema Habiby; Bernard Silverman; Robert Listernick; Joel Charrow
- Book ID
- 117165668
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 279 KB
- Volume
- 131
- Category
- Article
- ISSN
- 1097-6833
No coin nor oath required. For personal study only.
๐ 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