Neurofibromatosis type 1
β Scribed by Kevin P. Boyd; Bruce R. Korf; Amy Theos
- Book ID
- 116585474
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 471 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1097-6787
No coin nor oath required. For personal study only.
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
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
Growth abnormalities such as macrocephaly and short stature have been described and are considered a consistent finding in neurofibromatosis type 1 (NF1), one of the most common autosomal dominant disorders in man. We present here a clinical study on the growth profile of a sample of NF1 patients co