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WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations
Author(s) -
Suri Mohnish,
Kelehan Peter,
O'Neill David,
Vadeyar Shantala,
Grant Judith,
Ahmed S. Faisal,
Tolmie John,
McCann Emma,
Lam Wayne,
Smith Shirley,
FitzPatrick David,
Hastie Nicholas D.,
Reardon William
Publication year - 2007
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.31924
Subject(s) - biology , missense mutation , wilms' tumor , mutation , phenotype , diaphragmatic breathing , zinc finger , male pseudohermaphroditism , mesothelium , pathology , genetics , cancer research , gene , anatomy , endocrinology , medicine , peritoneum , alternative medicine , transcription factor
Meacham syndrome is a rare sporadically occurring multiple malformation syndrome characterized by male pseudohermaphroditism with abnormal internal female genitalia comprising a uterus and double or septate vagina, complex congenital heart defect and diaphragmatic abnormalities. We report on eight new cases of this condition, two of whom were shown to have heterozygous missense mutations in the C‐terminal zinc finger domains of WT1 : Arg366Cys and Arg394Trp. These data represent clinical and molecular evidence that the WT1 gene plays a central role in normal development of the diaphragm and the proepicardially derived tissues. Identification of WT1 expression in the region of coelomic mesothelium which will form the proepicardium and diaphragm provides a plausible unifying patterning defect in these cases. Interestingly, the Arg366Cys mutation has been previously reported in Denys–Drash syndrome and Arg394Trp mutation has been previously reported in both isolated Wilms tumor and Denys–Drash syndrome. This phenotypic diversity with a single mutation suggests there are other factors modulating all aspects of WT1 function during human development. If genetic modifiers of WT1 can be identified in animal models these become good candidate genes for the cases with Meacham syndrome we report on here where WT1 mutations cannot be identified. © 2007 Wiley‐Liss, Inc.