Foramina parietalia permagna: the ins and outs.
نویسنده
چکیده
Foramina parietalia permagna or enlarged parietal foramina are a rare variant estimated to be less than 1 in 25,000 cases. Out of 150 dry macerated skulls studied one skull showed 2 large parietal foramina measuring 17.38 x 27.67 mm (right) and 15.31 x 25.46 mm (left) in size. Between them, across the sagittal suture, was a transverse communicating suture interrupted by 3 very small wormian bones. There is no denial of the fact that this familial transmitted trait is caused by erratic ossification due to gene mutations. The clinical importance lies in these being markers for underlying neural or bone pathology or metabolic syndrome. The enlarged parietal foramina as expressed by the eyes at the back remain a curious anatomical but a definite clinico-pathological entity.
منابع مشابه
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.
Foramina parietalia permagna (FPP) is an autosomal dominant condition characterized by cranial defects of the parietal bones. It can be present as an isolated feature, but it is also one of the characteristics of a contiguous gene syndrome associated with deletions on chromosome 11p11-p12. One of the proteins known to be involved in skull development is the MSX2 homeobox protein. Previously, MS...
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ورودعنوان ژورنال:
- Folia morphologica
دوره 71 2 شماره
صفحات -
تاریخ انتشار 2012