Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital agenesis of the uterus and vagina in women with normal ovaries, phenotype and karyotype.1,3 The associated lung malformations described are practically anecdotal.1–4 We report a case of associated partial anomalous pulmonary venous drainage. The patient is a 19-year-old woman with MRKH, who referred frequent colds and...

Bilateral femoral agenesis is a rare anomaly.  To the best of our knowledge, only three cases of simple congenital anomaly and three cases associated with femoral facial syndrome have been reported.  Here, we describe a simple form of bilateral femoral agenesis observed in one of the 2 dead fetuses delivered after termination of a 24-week twin pregnancy of a normal mother.  Post-mortem x-ray ex...

Isolated absence of the ductus arteriosus is extremely rare condition although the ductus arteriosus may be hypoplastic or aplastic in association with other aortic arch anomalies. Authors described a case of isolated agenesis of the ductus arteriosus documented by postmortem examination of a newborn infant who died of pneumonia following operation for a large omphalocele. The heart showed vent...