Acrocephalopolysyndactyly, type 2 (ACPS 2): A rare genetic disorder characterized by premature closing of skull bones, craniofacial abnormalities, heart defects, growth retardation and other disorders. More detailed information about the symptoms, causes, and treatments of Acrocephalopolysyndactyly, type 2 (ACPS 2) is available below.
See full list of 43 symptoms of Acrocephalopolysyndactyly, type 2 (ACPS 2)
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