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The dentofacial features of Sanjad–Sakati syndrome: a case report

✍ Scribed by M. I. Al-Malik


Book ID
108828997
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
83 KB
Volume
14
Category
Article
ISSN
0960-7439

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## Abstract ## BACKGROUND Johnson‐McMillin syndrome (JMS) is a rare neuroectodermal disorder characterized by alopecia, ear malformations, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism. It is inherited in an autosomal dominant manner; however, the causative gene has