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Results 1 - 9 of 9 for Parietal foramina
  1. Enlarged parietal foramina 
    Enlarged parietal foramina is an inherited condition of impaired skull development. It is characterized by enlarged openings (foramina) in the parietal bones, ...
    https://medlineplus.gov/.../condition/enlarged-parietal-foramina - Genetics
  2. ALX4 gene 
    ... ALX4 gene have been found to cause enlarged parietal foramina type 2. This condition is characterized by enlarged ... before birth. In people with this condition, the parietal foramina remain open throughout life.The mutations that cause ...
    https://medlineplus.gov/genetics/gene/alx4 - Genetics
  3. MSX2 gene 
    ... gene have been identified in people with enlarged parietal foramina type 1. This condition is characterized by enlarged ... before birth. In people with this condition, the parietal foramina remain open throughout life.The mutations that cause ...
    https://medlineplus.gov/genetics/gene/msx2 - Genetics
  4. Potocki-Shaffer syndrome 
    ... the top and sides of the skull (enlarged parietal foramina). These abnormal openings form extra "soft spots" on ... Unlike the usual newborn soft spots, the enlarged parietal foramina remain open throughout life.The signs and symptoms ...
    https://medlineplus.gov/genetics/condition/potocki-shaffer-syndrome - Genetics
  5. Frontonasal dysplasia 
    ... the top and sides of the skull (enlarged parietal foramina). Males with this form of the condition often ... Basaran S, Uyguner ZO. Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations. Am J Med ...
    https://medlineplus.gov/genetics/condition/frontonasal-dysplasia - Genetics
  6. Chromosome 11 
    ... the top and sides of the skull (enlarged parietal foramina), multiple noncancerous bone tumors called osteochondromas, intellectual disability, ... deletion of a gene called ALX4 causes enlarged parietal foramina in people with this condition, loss of the ...
    https://medlineplus.gov/genetics/chromosome/11 - Genetics
  7. PHF21A gene 
    ... the top and sides of the skull (enlarged parietal foramina) and multiple noncancerous bone tumors (osteochondromas). Other signs ... chromosome 11, ALX4 and EXT2, underlie the enlarged parietal foramina and multiple osteochondromas, respectively. The loss of additional ...
    https://medlineplus.gov/genetics/gene/phf21a - Genetics
  8. EXT2 gene 
    ... the top and sides of the skull (enlarged parietal foramina). Other signs and symptoms seen in some people ... loss of the ALX4 gene results in enlarged parietal foramina, and deletion of the PHF21A gene causes intellectual ...
    https://medlineplus.gov/genetics/gene/ext2 - Genetics
  9. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
    https://medlineplus.gov/craniofacialabnormalities.html - Health Topics