Affiliation:
1. Department of Pediatrics, University of Pittsburgh School of Medicine
Abstract
Two infants have been described who exhibited previously unreported urogenital anomalies. Both patients were female pseudohermaphrodites of non-adrenal origin who had persistent cloacae.
The etiology of the anomalies is unknown. This rare combination of anomalies was recognizable clinically. If the diagnosis is made promptly, surgical correction may possibly prevent serious renal damage.
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology and Child Health
Cited by
3 articles.
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