Acrocephalopolysyndactyly (ACPS) syndrome is comprised of a rare group of disorders collectively characterised by:
- calvarial anomalies: e.g. craniosynostoses
- digital anomalies: syndactyly and polydactyly
While there can be some overlap in features, they can be primarily classified into the following major types
- type I: Noack syndrome
- type II: Carpenter syndrome (most common 1)
- type III: Sakati-Nyhan syndrome
- type IV: Goodman syndrome
See also
- acrocephalosyndactyly syndromes (when there is no polydactyly)