Sanjad-Sakati syndrome (SSS) is a rare autosomal recessive disorder seen in children of Middle Eastern descent, predominantly of consanguineous parents. This disorder has been mapped to the long arm of chromosome 1 (1q42-q43) and is caused by mutations in the TBCE gene (OMIM 241410), encoding a tubulin-specific chaperone E.1
Tanna N, Preciado DA, Biran N. The Otolaryngologic Features of Sanjad-Sakati Syndrome. Arch Otolaryngol Head Neck Surg. 2009;135(7):714–715. doi:10.1001/archoto.2009.76
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