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Parietal foramina 2
- ... Testing Registry: Parietal foramina 1 Genetic Testing Registry: Parietal foramina 2 National Organization for Rare Disorders (NORD) PARIETAL FORAMINA 1; PFM1 PARIETAL FORAMINA 2; PFM2 PubMed Edwards LS, Sachs JR, Elster AD. ...
- ... 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. ...
- ... 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 ...
- ... the top and sides of the skull (enlarged parietal foramina). These abnormal openings form extra "soft spots" on the head, in addition to the two that newborns normally have. Unlike the usual newborn ...
- ... 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 ...
- ... loss (alopecia) and an enlarged opening in the two bones that make up much of the top and sides of the skull (enlarged parietal foramina). Males with this form of the condition often ...
- ... 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 ...
- ... Potocki-Shaffer syndrome include enlarged openings in the two bones that make up much of the top and sides of the skull (enlarged parietal foramina), multiple noncancerous bone tumors called osteochondromas, intellectual disability, ...