Acropectoral syndrome

Acro-pectoral syndrome is characterized by a combination of distal limb abnormalities (syndactyly of all fingers and toes, preaxial polydactyly in the feet and/or hands) and upper sternum malformations. It has been described in 22 patients from a six-generation Turkish family. It is transmitted as an autosomal dominant trait and the causative gene is located at 7q36.

Also known as: ACRP syndrome, acropectoral syndrome, syndactyly-preaxial polydactyly-sternal deformity syndrome, ACRPS, Dundar Acropectoral syndrome, acro-pectoral syndrome, syndactyly, preaxial polydactyly and sternal deformity, syndactyly, preaxial polydactyly, and sternal deformity

1 clinical trial for this condition and its sub-types, 0 tagged with Acropectoral syndrome itself.