Parietal Foramina With Clavicular Hypoplasia

Watchlist
Retrieved
2021-01-23
Source
Trials
Genes
Drugs

A rare genetic bone development disorder characterized by parietal foramina in association with hypoplasia of the clavicles (short abnormal clavicles with tapering lateral ends, with or without loss of the acromion). Additional features may include mild craniofacial dysmorphism (macrocephaly, broad forehead and frontal bossing). No dental abnormalities were reported.