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Am J Med Genet A. 2006 Jun 1;140(11):1223-7.

A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype.

Author information

1
Institute of Human Genetics, University of Leipzig--Medical Faculty, Leipzig, Germany. heinw@medizin.uni-leipzig.de

Abstract

Mowat-Wilson syndrome (MWS) is a rare mental retardation-multiple congenital anomalies syndrome associated with typical facial dysmorphism. Patients can show a variety of other anomalies like short stature, microcephaly, Hirschsprung disease, malformations of the brain, seizures, congenital heart defects and urogenital anomalies. Mutations leading to haploinsufficiency of the ZFHX1B gene have been described as the underlying cause of this condition. We report on the clinical findings in a 2(1/2)-year-old boy with some aspects out of the MWS-spectrum in addition to unusual anomalies and a novel missense mutation in the ZFHX1B gene.

PMID:
16688751
DOI:
10.1002/ajmg.a.31267
[Indexed for MEDLINE]

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