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Results 1 - 4 of 4 for Parietal foramina 2
  1. ALX4 gene 
    ... ALX4 gene have been found to cause enlarged parietal foramina type 2. This condition is characterized by enlarged openings (foramina) ... Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome. Am J Hum Genet. ...
    https://medlineplus.gov/genetics/gene/alx4 - Genetics
  2. MSX2 gene 
    ... bone in areas of the skull and enlarged parietal foramina. More About This Health Condition At least two mutations in the MSX2 gene cause a condition ...
    https://medlineplus.gov/genetics/gene/msx2 - Genetics
  3. EXT2 gene 
    ... loss of the ALX4 gene results in enlarged parietal foramina, and deletion of the PHF21A gene causes intellectual disability and distinctive facial features. More About This Health Condition At least two mutations in the EXT2 gene have been found ...
    https://medlineplus.gov/genetics/gene/ext2 - Genetics
  4. PHF21A gene 
    ... People with this condition have enlarged openings in two bones that make up much of the top and sides of the skull (enlarged parietal foramina) and multiple noncancerous bone tumors (osteochondromas). Other signs ...
    https://medlineplus.gov/genetics/gene/phf21a - Genetics