Goodman syndrome

Goodman syndrome is an extremely rare genetic disorder characterized by marked malformations of the head and face (essentially acrocephaly), abnormalities of the hands and feet (polydactyly, syndactyly, clinodactyly, camptodactyly, ulnar deviation), and congenital heart disease. There have been no further descriptions in the literature since 1979. Goodman syndrome could be a variant of Carpenter syndrome.

Also known as: ACPS 4, ACPS4, Goodman syndrome, acrocephalopolysyndactyly type 4, Goodman camptodactyly, acrocephalopolysyndactyly type IV

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