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Results 1 - 10 of 11 for Craniosynostosis
  1. FGFR2 gene 
    ... premature closure of the bones of the skull (craniosynostosis), leading to a misshapen head, distinctive facial features, ... Stevenson cutis gyrata syndrome, a condition that causes craniosynostosis, leading to a misshapen head and distinctive facial ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  2. MSX2 gene 
    ... in the MSX2 gene cause a condition called craniosynostosis type 2 (also known as Boston type craniosynostosis). Craniosynostosis involves premature closure of the bones of ...
    https://medlineplus.gov/genetics/gene/msx2 - Genetics
  3. FGFR3 gene 
    ... premature joining of the bones of the skull (craniosynostosis), leading to a misshapen head and distinctive facial ... Muenke syndrome, which is a condition that causes craniosynostosis and leads to a misshapen head and distinctive ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  4. TWIST1 gene 
    ... by the premature fusion of certain skull bones (craniosynostosis), which prevents the skull from growing normally and ... also been found in several people with isolated craniosynostosis, which is a premature fusion of certain skull ...
    https://medlineplus.gov/genetics/gene/twist1 - Genetics
  5. RECQL4 gene 
    ... including the abnormal fusion of certain skull bones (craniosynostosis), small stature, missing thumbs or bones in the ... Gillerot Y, Megarbane A, Verloes A. Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused ...
    https://medlineplus.gov/genetics/gene/recql4 - Genetics
  6. FGFR1 gene 
    ... premature fusion of certain bones in the skull (craniosynostosis). They may also lack teeth, or their teeth ... cause Pfeiffer syndrome. This condition is characterized by craniosynostosis, which leads to a misshapen head and distinctive ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  7. PTCH1 gene 
    ... Hudgins L. Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay. Am J Med ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  8. EFNB1 gene 
    ... premature closure of certain bones of the skull (craniosynostosis) during development, which affects the shape of the ...
    https://medlineplus.gov/genetics/gene/efnb1 - Genetics
  9. SLC25A24 gene 
    ... U. De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. ...
    https://medlineplus.gov/genetics/gene/slc25a24 - Genetics
  10. FBN1 gene 
    ... J, Bennetts B. FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited. Am J Med Genet ...
    https://medlineplus.gov/genetics/gene/fbn1 - Genetics
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