Cerebral ganglioglioma and neurofibromatosis type I
โ Scribed by P. M. Parizel; J. -J. Martin; M. Vyve; L. Hauwe; A. M. Schepper
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 926 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0028-3940
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Neurofibromatosis type 1 (NF1), or von Recklinghausen disease is a genetic disease characterized by a variety of multiple clinical symptoms affecting primarily cells of neural crest origin, and is therefore classified as neurocristopathy. The most clinically significant feature of the disease is the
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