Literature DB >> 25008444

Mosaic generalized neurofibromatosis 1: report of two cases.

Jori Hardin, Allan Behm, Richard M Haber.   

Abstract

BACKGROUND: We report two cases of mosaic generalized neurofibromatosis 1 (NF1) and review the history of the classification of segmental neurofibromatosis (SNF; Ricardi type NF-V). Somatic mutations giving rise to limited disease, such as segmental neurofibromatosis are manifestations of mosaicism. If the mutation occurs before tissue differentiation, the clinical phenotype will be generalized disease. Mutations that occur later in development give rise to disease that is confined to a single region.
OBJECTIVES: Segmental neurofibromatosis is caused by a somatic mutation of neurofibromatosis type 1, and should not be regarded as a distinct entity from neurofibromatosis 1. Cases previously referred to as unilateral or bilateral segmental neurofibromatosis are now best referred to as mosaic generalized or mosaic localized neurofibromatosis 1.

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Year:  2014        PMID: 25008444     DOI: 10.2310/7750.2013.13116

Source DB:  PubMed          Journal:  J Cutan Med Surg        ISSN: 1203-4754            Impact factor:   2.092


  1 in total

1.  Segmental neurofibromatosis with deep schwannoma.

Authors:  Wallace A Smith; Brittany A Buhalog; Katherine H Fiala
Journal:  Indian Dermatol Online J       Date:  2016 Nov-Dec
  1 in total

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