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Results 1 - 3 of 3 for Abnormality of skull ossification
  1. TRIP11 gene 
    ... easily, and a lack of normal bone formation (ossification) in the skull, spine, and pelvis. Serious health problems result from these abnormalities, and infants with achondrogenesis usually die before or ...
    https://medlineplus.gov/genetics/gene/trip11 - Genetics
  2. ALX4 gene 
    ... ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). J Med Genet. ...
    https://medlineplus.gov/genetics/gene/alx4 - Genetics
  3. FGFR3 gene 
    ... causes premature joining of the bones of the skull (craniosynostosis), leading to a misshapen head and distinctive facial features. It also causes a skin abnormality called acanthosis nigricans that is characterized by thick, ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics