8p23.1 microdeletion syndrome

8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterized by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects.

Also known as: Del(8)(p23.1), monosomy 8p23.1, 8p23.1 deletion, chromosome 8p23.1 deletion, deletion 8p23.1

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