Neurofibromatosis type 1--an update and review for the primary pediatrician.

Abstract:

:With an incidence of 1 in 3,000, neurofibromatosis type 1 (NF1), or von Recklinghausen disease, is one of the most common genetic disorders encountered by primary care physicians. NF1 is a multisystem disease that affects more than one million people worldwide (more than 80,000 in the United States). Although most pediatricians have patients with NF1 in their practices, many affected individuals go undiagnosed as children. This article is intended to facilitate the diagnosis and management of young patients with NF1.

journal_name

Clin Pediatr (Phila)

journal_title

Clinical pediatrics

authors

Goldberg Y,Dibbern K,Klein J,Riccardi VM,Graham JM Jr

doi

10.1177/000992289603501101

subject

Has Abstract

pub_date

1996-11-01 00:00:00

pages

545-61

issue

11

eissn

0009-9228

issn

1938-2707

journal_volume

35

pub_type

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