Denys-Drash syndrome: Difference between revisions
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'''Denys-Drash syndrome''' a constellation of findings due to a mutation in the ''WT1 gene''.<ref name=omim607102>{{OMIM|607102}}</ref> | '''Denys-Drash syndrome''', abbreviated '''DDS''', is a constellation of findings due to a mutation in the ''WT1 gene''.<ref name=omim607102>{{OMIM|607102}}</ref> | ||
Classically, it is characterized by the triad:<ref name=omim194080>{{OMIM|194080}}</ref> | Classically, it is characterized by the triad:<ref name=omim194080>{{OMIM|194080}}</ref> | ||
Revision as of 12:50, 24 September 2013
Denys-Drash syndrome, abbreviated DDS, is a constellation of findings due to a mutation in the WT1 gene.[1]
Classically, it is characterized by the triad:[2]
- Nephropathy.
- Wilms tumour.
- Genital abnormalities.