Diprosopus

MONDO:0015672

Diprosopus is a rare, life-threatening developmental defect during embryogenesis, and a subtype of conjoined twins, characterized by partial or complete duplication of the facial structures on a single head, neck, trunk and body. It may be associated with congenital anomalies involving the central nervous, cardiovascular, gastrointestinal and respiratory systems. Cleft lip and palate have been reported in rare cases.

Also known as: Diprosopia, craniofacial duplication

0 clinical trials for this condition and its sub-types, 0 tagged with Diprosopus itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Disorder of development or morphogenesis (5170)

Including sub-types (0) Tagged with Diprosopus (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.