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[Maxillo-facial abnormalities in Kearns-Sayre syndrome].

作者信息

Piazzi A, Berio A

机构信息

Cattedra di Pediatria, Universìtà di Genova.

出版信息

Pediatr Med Chir. 2003 Jan-Feb;25(1):53-7.

Abstract

Three cases of Kearns-Sayre Syndrome are reported, in which some facial anomalies, including facial asymmetry, high forehead, wide nasal bridge, upturned nose, flat philtrum, low set ears and short neck were present. In two cases, the diagnosis of oxidative phosphorylation deficiency was confirmed by hystoenzymatic and genetic studies. The relationship of these facial anomalies with neural crest maldevelopment is emphasized and a classification of the Kearns-Sayre Syndrome as metabolic neurocristopathy is proposed. The facial anomalies are suggestive of an antenatal expression of the oxidative phosphorylation disease.

摘要

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