HIGHLIGHTS
- What: The authors report a case of an 18-year-old female patient born to consanguineous parents who had never been diagnosed with NF1 nor had any of her family members.
- Who: Wael A. Alsakran and colleagues from the College of Medicine, University of Jeddah, Jeddah, Ophthalmology, College of Medicine have published the research: Review began 11/16/2024 Review ended 12/02/2024 Published 12/05/2024 © Copyright, in the Journal: (JOURNAL) of December/05,/2024
SUMMARY
Neurofibromatosis type 1 (NF1) is an autosomal dominant phakomatosis described phenotypically by von . . .
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