Pseudohermaphroditism, glomerulopathy and Wilms' tumour (Drash syndrome): a case report

J M Hutson; G Werther

doi:10.1111/j.1440-1754.1990.tb02436.x

Pseudohermaphroditism, glomerulopathy and Wilms' tumour (Drash syndrome): a case report

J Paediatr Child Health. 1990 Aug;26(4):227-9. doi: 10.1111/j.1440-1754.1990.tb02436.x.

Authors

J M Hutson¹, G Werther

Affiliation

¹ Department of Paediatrics, University of Melbourne, Victoria, Australia.

PMID: 2175210
DOI: 10.1111/j.1440-1754.1990.tb02436.x

Abstract

A baby with ambiguous genitalia and 46XY chromosomes was raised as a female. Sudden and unexpected death at 11 months of age led to a post-mortem diagnosis of Drash syndrome.

Publication types

Case Reports

MeSH terms

Diagnostic Errors
Disorders of Sex Development / diagnosis*
Female
Humans
Infant, Newborn
Kidney Diseases / diagnosis*
Kidney Neoplasms / diagnosis*
Syndrome
Wilms Tumor / diagnosis*