Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 6 of 6 for acrocephalosyndactyly
  1. Apert syndrome 
    ... no history of the disorder in their family. Acrocephalosyndactyly Acrocephalosyndactyly type I Apert's syndrome Type I acrocephalosyndactyly Genetic Testing Registry: Acrocephalosyndactyly type I Apert syndrome ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  2. Carpenter syndrome 
    ... condition. ACPS II Acrocephalopolysyndactyly 2 Acrocephalopolysyndactyly type II Acrocephalosyndactyly, type II Type II acrocephalosyndactyly Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/carpenter-syndrome - Genetics
  3. TWIST1 gene 
    ... in the skull and leads to isolated craniosynostosis. acrocephalosyndactyly 3 ACS3 B-HLH DNA binding protein CRS1 ... transcription factor 1 Twist Homolog twist homolog 1 (acrocephalosyndactyly 3; Saethre-Chotzen syndrome) (Drosophila) twist homolog 1 ( ...
    https://medlineplus.gov/genetics/gene/twist1 - Genetics
  4. Apert syndrome 
    Apert syndrome is a genetic disease in which the seams between the skull bones close earlier than normal. This affects the shape of ...
    https://medlineplus.gov/ency/article/001581.htm - Medical Encyclopedia
  5. Pfeiffer syndrome 
    ... each cell is sufficient to cause the disorder. Acrocephalosyndactyly, type V ACS V ACS5 Craniofacial-skeletal-dermatologic ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics
  6. Saethre-Chotzen syndrome 
    ... other typical signs and symptoms of the condition. Acrocephalosyndactyly III Acrocephalosyndactyly, type III Acrocephaly, skull asymmetry, and mild syndactyly ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics