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Results 1 - 10 of 23 for Craniosynostosis 4
  1. 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
  2. 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
  3. 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
  4. 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. Erratum In: J Appl ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  5. Jackson-Weiss syndrome 
    ... 275. Erratum In: Nat Genet 1995 Apr;9(4):451. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics
  6. 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
  7. 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
  8. Baller-Gerold syndrome 
    ... Sklower SL, Willner JP, Desnick RH, Cohen MM. Craniosynostosis-radial aplasia: ... Childs Nerv Syst. 2006 Jan;22(1):90-4. doi: 10.1007/s00381-004-1089-x. Epub ...
    https://medlineplus.gov/genetics/condition/baller-gerold-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. Craniofrontonasal syndrome 
    ... premature closure of certain bones of the skull (craniosynostosis) during development, which affects the shape of the ... Yesodharan D, Udayakumaran S, Subash P, Kornak U. Four novel mutations in EFNB1 in Indian patients with ...
    https://medlineplus.gov/.../condition/craniofrontonasal-syndrome - Genetics
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