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Results 1 - 10 of 43 for Craniosynostosis 4
  1. Baby's Head Shape: Cause for Concern? (Mayo Foundation for Medical Education and Research)  
    Infant and Newborn Care/Related Issues ... Infant and Newborn Care ... Craniofacial Abnormalities/Related Issues ... Craniofacial Abnormalities ... Mayo Foundation for Medical ...
    https://www.mayoclinic.org/.../healthy-baby/art-20045964?p=1 - External Health Links
  2. Muenke syndrome 
    ... 000 newborns. This condition accounts for an estimated 4 percent of all cases of craniosynostosis. A particular mutation in the FGFR3 gene causes ...
    https://medlineplus.gov/genetics/condition/muenke-syndrome - Genetics
  3. 19p13.13 deletion syndrome 
    ... S, Thorland EC, Khorasani L, Reid RR. Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12-19p13.2. Genes Dis. 2015 Dec;2(4):347-352. doi: 10.1016/j.gendis.2015. ...
    https://medlineplus.gov/genetics/condition/19p1313-deletion-syndrome - Genetics
  4. Craniosynostosis 
    ... P, Nash H. Impact of surgery timing for craniosynostosis on neurodevelopmental outcomes: a systematic review. J Neurosurg Pediatr. 2019;23(4):442-454. PMID: 30684935 pubmed.ncbi.nlm.nih. ...
    https://medlineplus.gov/ency/article/001590.htm - Medical Encyclopedia
  5. 22q11.2 deletion syndrome 
    ... LaRossa D, Bartlett SP, Whitaker LA, Zackai EH. Craniosynostosis: another feature of the 22q11.2 deletion syndrome. Am J Med Genet A. 2005 Aug 1;136A(4):358-62. doi: 10.1002/ajmg.a.30746. ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  6. Chromosome 15 
    ... chromosome 15: confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome. Am J Med Genet. 1999 Dec 22;87(5):391-4. doi: 10.1002/(sici)1096-8628(19991222)87: ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  7. Apert syndrome 
    ... PubMed Kutkowska-Kazmierczak A, Gos M, Obersztyn E. Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling. J Appl Genet. 2018 May;59(2):133-147. doi: 10.1007/s13353-017-0423-4. Epub 2018 Feb 1. Citation on PubMed Surman ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  8. 3MC syndrome 
    ... abnormal fusion of certain bones in the skull (craniosynostosis) or forearm ... encompasses four disorders that were formerly considered to be separate: ...
    https://medlineplus.gov/genetics/condition/3mc-syndrome - Genetics
  9. Beare-Stevenson cutis gyrata syndrome 
    ... Am J 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
  10. 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
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