Neurofibromatosis 1: A family case series

Neurofibromatosis 1: A family case series

Neurofibromatosis type 1 (NF1) or Von Recklinghausen disease comes under a group of multisystem hereditary syndromes called phakomatoses. It presents with skin, ophthalmic, bony, and systemic manifestations. We present a photographically well-documented case series of NF in a family (n = 3). Skin ma...

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Bibliographic Details
Main Authors: Neha K Sethi, Charu Chadha, Sumit Goyal, Manpreet Kaur
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Journal of Family Medicine and Primary Care
Subjects:
familial
hereditary
lisch nodules
mechanical ectropion
mechanical ptosis
neurofibroma
von recklinghausen disease
Online Access:http://www.jfmpc.com/article.asp?issn=2249-4863;year=2022;volume=11;issue=5;spage=2252;epage=2255;aulast=Sethi

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http://www.jfmpc.com/article.asp?issn=2249-4863;year=2022;volume=11;issue=5;spage=2252;epage=2255;aulast=Sethi

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