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Results 1 - 8 of 8 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. Enlarged parietal foramina 
    ... that form the top and sides of the skull. This condition is due to incomplete bone formation (ossification) within the parietal bones. The openings are symmetrical ...
    https://medlineplus.gov/.../condition/enlarged-parietal-foramina - Genetics
  4. Achondrogenesis 
    ... typically have ribs that fracture easily. Bone formation (ossification) is also severely reduced in the skull and spine.Infants with achondrogenesis type 1B, which ...
    https://medlineplus.gov/genetics/condition/achondrogenesis - Genetics
  5. 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
  6. Osteoporosis-pseudoglioma syndrome 
    ... carriers may have decreased bone mineral density. OPPG Osteogenesis imperfecta, ocular form Genetic Testing Registry: Osteoporosis with ...
    https://medlineplus.gov/.../osteoporosis-pseudoglioma-syndrome - Genetics
  7. Achondroplasia 
    ... of the hole at the base of the skull where the spinal cord comes out of brain (foramen ... Achondroplasia is the most common type of short- ...
    https://medlineplus.gov/genetics/condition/achondroplasia - Genetics
  8. Cleidocranial dysplasia 
    ... is later converted to bone (a process called ossification), except for the cartilage that continues to cover ... Stoddart MJ. Role and regulation of RUNX2 in osteogenesis. Eur Cell Mater. 2014 Oct 23;28:269- ...
    https://medlineplus.gov/genetics/condition/cleidocranial-dysplasia - Genetics