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Results 1 - 10 of 42 for Craniosynostosis 7
  1. TWIST1 gene 
    ... Speltz ML, Cunningham ML. Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations. Am J Med Genet A. 2007 Apr 1;143A(7):678-86. doi: 10.1002/ajmg.a.31630. ...
    https://medlineplus.gov/genetics/gene/twist1 - Genetics
  2. Chromosome 7 
    ... by the premature fusion of certain skull bones (craniosynostosis), which prevents the skull from growing normally and affects the shape of the head and face. The chromosomal changes involve a region of the short (p) arm of chromosome 7 that contains the TWIST1 gene. This gene plays ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  3. Apert syndrome 
    ... Hayward RD, Jones BM. The elbow in syndromic craniosynostosis. J Craniofac ... 1999 Jul-Aug;19(4):504-7. doi: 10.1097/00004694-199907000-00015. Citation on ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  4. Beare-Stevenson cutis gyrata syndrome 
    ... Med Genet A. 2015 Apr;167A(4):852-7. doi: 10.1002/ajmg.a.36985. Epub 2015 Feb 23. Citation on PubMed
    https://medlineplus.gov/.../beare-stevenson-cutis-gyrata-syndrome - Genetics
  5. Craniosynostosis repair 
    Craniosynostosis repair is surgery to correct a problem that causes the bones of a child's skull to ... open, the baby's skull and brain can grow. Craniosynostosis is a condition that causes one or more ...
    https://medlineplus.gov/ency/article/007364.htm - Medical Encyclopedia
  6. Mowat-Wilson syndrome 
    ... L, Zollino M, Zackai EH. CHARGE-like presentation, craniosynostosis and mild ... 2015 Jul;167(7):1682-3. Citation on PubMed Wilson M, Mowat ...
    https://medlineplus.gov/genetics/condition/mowat-wilson-syndrome - Genetics
  7. Craniosynostosis repair - discharge 
    Craniosynostosis repair is surgery to correct a problem that causes the bones of a child's skull to ... Your child was diagnosed with craniosynostosis. This is a condition that causes one or more of your child's skull sutures (the junction of two skull bones) to ...
    https://medlineplus.gov/ency/patientinstructions/000067.htm - Medical Encyclopedia
  8. Shprintzen-Goldberg syndrome 
    ... Am J Med Genet A. 2012 Jul;158A(7):1574-8. doi: 10.1002/ajmg.a.35388. Epub 2012 May 25. Citation on PubMed Sood S, Eldadah ZA, Krause WL, McIntosh I, Dietz HC. Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome. Nat Genet. 1996 Feb;12( ...
    https://medlineplus.gov/.../condition/shprintzen-goldberg-syndrome - Genetics
  9. Carpenter syndrome 
    ... by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, and other developmental problems.Craniosynostosis prevents the skull from growing normally, frequently giving ...
    https://medlineplus.gov/genetics/condition/carpenter-syndrome - Genetics
  10. Saethre-Chotzen syndrome 
    ... by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing ... similar to those of Saethre-Chotzen syndrome, including craniosynostosis and broad or duplicated great toes. It was ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics
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