HIGHLIGHTS
- who: Dysembryoplasia and collaborators from the Ophthalmology, University of Medicine and Pharmacy have published the research: Neurofibromatosis Type 1, Von Recklinghausen Disease - Clinical Features, in the Journal: (JOURNAL) of July/18,/2022
- what: NF1 is a multisystem genetic condition with autosomal dominant transmission, which has variable clinical aspects and has a serious evolution, sometimes life-threatening.
SUMMARY
Neurofibromatosis is the most common phacomatosis with an incidence of 1/3000 cases. Neurofibromatosis type 1 - NF1 - or von Recklinhausen`s disease is a polymorphic condition with variable clinical features, evolutionary, severe, sometimes life . . .
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