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Goodman syndrome
rareGoodman 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.
- Identifiers
- MONDO:0008711 OMIM:201020Orphanet:65798
- Part of
- AcrocephalopolysyndactylyMultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
- Also known as
- ACPS 4 · ACPS4 · acrocephalopolysyndactyly type 4 · Goodman camptodactyly
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