The occurrence of both PFM and clavicular hypoplasia is known as parietal foramina with cleidocranial dysplasia (PFMCCD). It is listed as a separate entity in both OMIM (168550) and the London ...
Parietal foramina (PFM) [MIM 168500] is an extremely rare congenital developmental anomaly of the parietal bone. The hereditary mode is usually autosomal dominant. PFM is characterized by symmetrical, ...
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