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Results 1 - 10 of 64 for Craniosynostosis 2
  1. MSX2 gene 
    ... Tests of MSX2 PubMed MSH HOMEOBOX 2; MSX2 CRANIOSYNOSTOSIS 2; CRS2 NCBI Gene ClinVar Florisson JM, Verkerk AJ, Huigh D, Hoogeboom AJ, Swagemakers S, Kremer A, Heijsman D, Lequin MH, Mathijssen IM, van der Spek PJ. Boston type craniosynostosis: report of a second mutation in MSX2. Am ...
    https://medlineplus.gov/genetics/gene/msx2 - Genetics
  2. 19p13.13 deletion syndrome 
    ... E, Sibille C. A new case of syndromic craniosynostosis with cryptic 19p13.2-p13.13 deletion. Am J Med Genet A. ...
    https://medlineplus.gov/genetics/condition/19p1313-deletion-syndrome - Genetics
  3. Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDF  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
    https://ccakids.org/.../uploads/2022/01/pfeiffer-guide_2018.pdf - External Health Links
  4. Carpenter syndrome 
    ... results in a deformity called a cloverleaf skull. Craniosynostosis can cause differences between the two sides of the head and face (craniofacial asymmetry). ...
    https://medlineplus.gov/genetics/condition/carpenter-syndrome - Genetics
  5. Crouzon syndrome 
    ... Growth Factor Receptor 2 (FGFR2) Mutation Related Syndromic Craniosynostosis. Int J Biol Sci. 2017 Nov 2;13(12):1479-1488. doi: 10.7150/ijbs. ...
    https://medlineplus.gov/genetics/condition/crouzon-syndrome - Genetics
  6. FGFR2 gene 
    ... Growth Factor Receptor 2 (FGFR2) Mutation Related Syndromic Craniosynostosis. Int J Biol Sci. 2017 Nov 2;13(12):1479-1488. doi: 10.7150/ijbs. ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  7. 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 ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  8. Baller-Gerold syndrome 
    ... K, Gunning L, Bloom AD. Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome. Clin Genet. 1980 Feb;17(2):161-6. doi: 10.1111/j.1399-0004. ... Gillerot Y, Megarbane A, Verloes A. Revisiting the craniosynostosis-radial ... gene. J Med Genet. 2006 Feb;43(2):148-52. doi: 10.1136/jmg.2005.031781. ...
    https://medlineplus.gov/genetics/condition/baller-gerold-syndrome - Genetics
  9. Shprintzen-Goldberg syndrome 
    ... HC. Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome. Nat Genet. 1996 Feb;12(2):209-11. doi: 10.1038/ng0296-209. Citation ...
    https://medlineplus.gov/.../condition/shprintzen-goldberg-syndrome - Genetics
  10. Saethre-Chotzen syndrome 
    ... ML, Ratisoontorn C, Heike CL, Hing AV. Syndromic craniosynostosis: from history to hydrogen bonds. Orthod Craniofac Res. 2007 May;10(2):67-81. doi: 10.1111/j.1601-6343. ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics
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