Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Fraser And Ablepharon Macrostomia Phenotypes: Concurrence In One Family And Association With Mutated Fras1.
Author: Cavalcanti, Denise Pontes
Matejas, Verena
Luquetti, Daniela
Mello, Marcos Fernando
Zenker, Martin
Abstract: To date, Fraser syndrome (FS) and Ablepharon macrostomia syndrome (AMS) have been considered distinct disorders, but they share strikingly similar patterns of congenital abnormalities, specifically craniofacial anomalies. While recent research has led to the identification of the genes FRAS1 and FREM2 as the cause of FS, the genetic basis of AMS continues to be enigmatic. We report on the concurrence of AMS-like and Fraser phenotypes in a Brazilian family. Both affected sibs were homozygous for a novel splice site mutation in the FRAS1 gene. Extensive studies on mRNA expression indicated that this mutation most likely leads to loss of function as most previously reported FRAS1 mutations associated with FS. We conclude that a phenotype resembling AMS is a rare clinical expression of FS with no obvious genotype-phenotype correlation. However, the molecular basis of true AMS which has been reported as a sporadic disorder in all cases but one, and so far with no relation to FS, is probably different and still needs to be further investigated.
Subject: Abnormalities, Multiple
Craniofacial Abnormalities
Extracellular Matrix Proteins
Infant, Newborn
Citation: American Journal Of Medical Genetics. Part A. v. 143A, n. 3, p. 241-7, 2007-Feb.
Rights: fechado
Identifier DOI: 10.1002/ajmg.a.31426
Date Issue: 2007
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File SizeFormat 
pmed_17163535.pdf313.76 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.