Otopalatodigital syndrome type 2

A severe form of otopalatodigital syndrome spectrum disorder, and is characterized by dysmorphic facies, severe skeletal dysplasia affecting the axial and appendicular skeleton, extraskeletal anomalies (including malformations of the brain, heart, genitourinary system, and intestine) and poor survival.

Also known as: OPD 2 syndrome, OPD II syndrome, OPD syndrome 2, Otopalatodigital Syndrome Type I and II, otopalatodigital syndrome, type II, X-linked dominant, Andre syndrome, FPO, OPD2

35 clinical trials for this condition and its sub-types.