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Results 1 - 8 of 8 for Parietal foramina 1
  1. ... Testing Registry: Cranium bifidum occultum Genetic Testing Registry: Parietal foramina 1 Genetic Testing Registry: Parietal foramina 2 Disease InfoSearch ...
  2. ... 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 ...
  3. ... 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. ...
  4. ... 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. ...
  5. ... 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 ...
  6. ... 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 ...
  7. ... 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 ...
  8. ... 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 ...