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Results 1 - 10 of 49 for Craniosynostosis syndrome
  1. Shprintzen-Goldberg syndrome 
    ... cells, it is known as germline mosaicism. Marfanoid-craniosynostosis syndrome Shprintzen-Goldberg craniosynostosis syndrome Genetic Testing Registry: Shprintzen- ...
    https://medlineplus.gov/.../condition/shprintzen-goldberg-syndrome - Genetics
  2. Muenke syndrome 
    ... some features overlap with those seen in other craniosynostosis syndromes. A small percentage of people with the gene ... PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/genetics/condition/muenke-syndrome - Genetics
  3. Beare-Stevenson cutis gyrata syndrome 
    ... Stevenson cutis gyrata syndrome Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome National Organization for Rare Disorders (NORD) BEARE-STEVENSON ...
    https://medlineplus.gov/.../beare-stevenson-cutis-gyrata-syndrome - Genetics
  4. Crouzon syndrome 
    ... per million newborns. It is the most common craniosynostosis syndrome. Mutations in the FGFR2 gene cause Crouzon syndrome. ... PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/genetics/condition/crouzon-syndrome - Genetics
  5. Baller-Gerold syndrome 
    ... of the condition. BGS Craniosynostosis with radial defects Craniosynostosis-radial aplasia syndrome Genetic Testing Registry: Baller-Gerold syndrome Baller-Gerold ...
    https://medlineplus.gov/genetics/condition/baller-gerold-syndrome - Genetics
  6. Apert syndrome 
    ... PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  7. Crouzon syndrome with acanthosis nigricans 
    ... PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/...rouzon-syndrome-with-acanthosis-nigricans - Genetics
  8. Jackson-Weiss syndrome 
    ... PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics
  9. Gorlin-Chaudhry-Moss syndrome 
    ... U. De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. Am ...
    https://medlineplus.gov/.../condition/gorlin-chaudhry-moss-syndrome - Genetics
  10. SLC25A24 gene 
    ... U. De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. Am ...
    https://medlineplus.gov/genetics/gene/slc25a24 - Genetics
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