acrocephalopolysyndactyly

Acrocephalopolysyndactyly (ACPS) syndrome is comprised of a rare group of disorders collectively characterized 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 )
• type III: Sakati-Nyhan syndrome
• type IV: Goodman syndrome

See also

• acrocephalosyndactyly syndromes (when there is no polydactyly)

Siehe auch:

• Polydaktylie
• Kraniosynostose
• Syndaktylie
• acrocephalosyndactyly
• Carpenter syndrome
• Noack syndrome
• Goodman syndrome
• Sakati Nyhan syndrome

und weiter:

• congenital syndromes associated with enlarged ventricles
• acrocephalopolysyndactyly type II
• acrocephalopolysyndactyly type III
• acrocephalopolysyndactyly type I