2q37 microdeletion syndrome

A chromosomal anomaly involving deletion of chromosome band 2q37 and manifests as three major clinical findings: developmental delay, skeletal malformations and facial dysmorphism.

Also known as: 2q37 microdeletion syndrome, 2q37 monosomy, Albright hereditary osteodystrophy type 3, Albright hereditary osteodystrophy-like syndrome, BDMR, Del(2)(q37), brachydactyly intellectual disability syndrome, brachydactyly mental retardation syndrome

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