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Results 1 - 4 of 4 for Parietal foramina 1
  1. MSX2 gene 
    ... gene have been identified in people with enlarged parietal foramina type 1. This condition is characterized by enlarged openings (foramina) in the parietal bones, which are the two bones that form ...
    https://medlineplus.gov/genetics/gene/msx2 - Genetics
  2. ALX4 gene 
    ... Basaran S, Uyguner ZO. Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations. Am J Med Genet A. 2012 Jan;158A(1):236-44. doi: 10.1002/ajmg.a.34390. ...
    https://medlineplus.gov/genetics/gene/alx4 - Genetics
  3. 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
  4. 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