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Renal dysplasia - megalocystis - sirenomelia

Orpha number ORPHA1850
Prevalence of rare diseases -
Inheritance -
Age of onset -
ICD 10 code -
MIM number -
Synonym(s) Selig-Benacerraf-Greene syndrome

Summary

This syndrome is characterized by bilateral renal agenesis or dysplasia, megacystis secondary to urethral obstruction and sirenomelia. It has been described in four siblings. The disorder is lethal. *Author: Orphanet (April 2007)*.

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