Apert syndrome

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Name:
Apert syndrome
Description:
A frequent form of acrocephalosyndactyly, a group of inherited congenital malformation disorders, characterized by craniosynostosis, midface hypoplasia, and finger and toe anomalies and/or syndactyly.
ORPHAcode:
87
Synonyms:
ACS1
Acrocephalosyndactyly type 1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14