Document Detail


HLXB9 homeobox gene and caudal regression syndrome.
MedLine Citation:
PMID:  16498628     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Caudal regression syndrome (CRS) is a congenital heterogeneous constellation of caudal anomalies that include varying degrees of agenesis of the spinal column, anorectal malformations (ARMs), genitourinary anomalies, and pulmonary hypoplasia. The combination of a particular form of hemisacrum, ARM, and presacral mass (teratoma, anterior meningocele, rectal duplication, or a combination thereof) constitutes Currarino syndrome (CS). Previous reports have shown HLXB9 to be a major causative gene for CS. The aim of our study was to reevaluate the involvement of the HLXB9 gene in a larger group of CRS cases. METHODS: SSCP analysis was performed on a series of 48 CRS cases without CS. A case-control approach was used to test whether an alteration of the length of the GCC triplets in exon 1 of the HLXB9 gene could contribute to CRS risk. RESULTS: No pathological variants of the HLXB9 gene were identified by mutational analysis. We also found no evidence that the length of the GCC triplets had any effect on the CRS risk, even when the allelic frequencies were stratified according to the presence or absence of ARMs and the type of sacral agenesis. CONCLUSIONS: We confirmed that the HLXB9 gene is not involved in the pathogenesis of CRS, and to date is known as a causative gene only for CS.
Authors:
Elisa Merello; Patrizia De Marco; Samantha Mascelli; Alessandro Raso; Maria Grazia Calevo; Michele Torre; Armando Cama; Margherita Lerone; Giuseppe Martucciello; Valeria Capra
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Birth defects research. Part A, Clinical and molecular teratology     Volume:  76     ISSN:  1542-0752     ISO Abbreviation:  Birth Defects Res. Part A Clin. Mol. Teratol.     Publication Date:  2006 Mar 
Date Detail:
Created Date:  2006-03-23     Completed Date:  2006-05-23     Revised Date:  2008-09-13    
Medline Journal Info:
Nlm Unique ID:  101155107     Medline TA:  Birth Defects Res A Clin Mol Teratol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  205-9     Citation Subset:  IM    
Copyright Information:
Copyright 2006 Wiley-Liss, Inc.
Affiliation:
U.O. Neurochirurgia, Istituto G. Gaslini, Genova, Italy.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple / epidemiology,  genetics*
Adolescent
Adult
Child
Child, Preschool
DNA Mutational Analysis
Female
Genetic Predisposition to Disease*
Homeodomain Proteins / genetics*,  metabolism
Humans
Italy / epidemiology
Lower Extremity Deformities, Congenital / epidemiology,  genetics*
Male
Polymorphism, Single-Stranded Conformational
Sacrum / abnormalities*
Syndrome
Transcription Factors / genetics*,  metabolism
Trinucleotide Repeats / genetics
Chemical
Reg. No./Substance:
0/Homeodomain Proteins; 0/MNX1 protein, human; 0/Transcription Factors
Comments/Corrections
Erratum In:
Birth Defects Res A Clin Mol Teratol. 2006 Jul;76(7):568

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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