Article
Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome.
Head & face medicine - 11 Dec 2019
Farrera Arodi, Villanueva María, Vizcaíno Alfredo, Medina-Bravo Patricia, Balderrábano-Saucedo Norma, Rives Mariana, Cruz David, Hernández-Carbajal Elizabeth, Granados-Riveron Javier, Sánchez-Urbina Rocío
Abstract excerpt
BACKGROUND: 22q11.2 deletion syndrome is a medical condition that results from genomic loss at chromosome 22. Affected patients exhibit large variability that ranges from a severe condition to mild symptoms. In addition, the spectrum of clinical features differs among populations and even within family members. The facial features related to this syndrome are not an exception, and although part of its variation...
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