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Published 1 April 2009
Cite this as: BMJ Case Reports 2009 [doi:10.1136/bcr.01.2009.1518]
Copyright © 2009 by the BMJ Publishing Group Ltd.

Unusual presentation of more common disease/injury

Potter syndrome with an unusual cardiac anomaly

Savit Prabhu1, Elanthenral Sigamani1, Prasenjit Das1, Arun Sasi2, Rajni Safaya1

1 Department of Pathology, All India Institute of Medical Sciences, New Delhi 110029, India
2 Department of Pediatrics, All India Institute of Medical Sciences, New Delhi 110029, India

Correspondence to:
R Safaya, prasenaiims{at}gmail.com

SUMMARY

Potter syndrome is a congenital anomaly characterised by bilateral renal agenesis, pulmonary hypoplasia, cardiac, skeletal abnormalities and maternal oligohydramnios. Here we report a case of Potter syndrome with bilateral renal agenesis, pulmonary hypoplasia and complete transposition of the great vessels, which had been identified during a post-mortem examination. Although cardiac anomalies are known to exist with Potter syndrome, complete transposition of the great vessels has not been reported in the literature.


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