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Darmency-Stamboul, Véronique; Burglen, Lydie; Lopez, Estelle; Mejean, Nathalie; Dean, John; Franco, Brunella; Rodriguez, Diana; Lacombe, Didier; Desguerres, Isabelle; Cormier-Daire, Valérie; Doray, Bérénice; Pasquier, Laurent; Gonzales, Marie; Pastore, Matthew; Crenshaw, Melissa L; Huet, Frédéric; Gigot, Nadège; Aral, Bernard; Callier, Patrick; Faivre, Laurence; Attié-Bitach, Tania; Thauvin-Robinet, Christel
European journal of medical genetics, 06/2013, Letnik: 56, Številka: 6Journal Article
Abstract Oral-facial-digital syndrome type VI (OFD VI) is characterized by the association of malformations of the face, oral cavity and extremities, distinguished from the 12 other OFD syndromes by cerebellar and metacarpal abnormalities. Cerebellar malformations in OFD VI have been described as a molar tooth sign (MTS), thus, including OFD VI among the “Joubert syndrome related disorders” (JSRD). OFD VI diagnostic criteria have recently been suggested: MTS and one or more of the following: 1) tongue hamartoma(s) and/or additional frenula and/or upper lip notch; 2) mesoaxial polydactyly of hands or feet; 3) hypothalamic hamartoma. In order to further delineate this rare entity, we present the neurological and radiological data of 6 additional OFD VI patients. All patients presented oral malformations, facial dysmorphism and distal abnormalities including frequent polydactyly (66%), as well as neurological symptoms with moderate to severe mental retardation. Contrary to historically reported patients, mesoaxial polydactyly did not appear to be a predominant clinical feature in OFD VI. Sequencing analyzes of the 14 genes implicated in JSRD up to 2011 revealed only an OFD1 frameshift mutation in one female OFD VI patient, strengthening the link between these two oral-facial-digital syndromes and JSRD.
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in: SICRIS
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