Apert syndrome
Name: |
Apert syndrome
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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.
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ORPHAcode: |
87
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Synonyms: |
ACS1
Acrocephalosyndactyly type 1
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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