Meacham syndrome

Meacham syndrome is a multiple malformation syndrome characterized by congenital diaphragmatic abnormalities, genital defects and cardiac malformations.

Also known as: Meacham syndrome, Meacham-Winn-Culler syndrome, Rhabdomyomatous dysplasia-cardiopathy-genital anomalies syndrome, Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype, Meacham Winn Culler syndrome

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