Search results for "Syndromes oro-facio-digitaux"

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Identification of molecular and physiopathologic basis in oral-facial-digital syndromes

2016

Oral-facial-digital syndromes (OFDS) are characterized by the association of oral, facial and digital anomalies. The different modes of inheritance and additional features lead to clinically delineate 13 subtypes. For a long time, only the OFD1 gene, responsible for OFDI subtype and coding for a centrosomal protein, has been known, suggesting the involvement of the primary cilium in OFDS. Mutations have recently been reported in the TMEM216, DDX59, SCLT1, TBC1D32 and TCTN3 genes in anecdotic cases. To identify new genes involved in OFDS, we performed whole-exome sequencing in 24 patients. In 14/24 cases, we identified 5 novel genes (C2CD3, TMEM107, INTU, KIAA0753, IFT57), enlarged the clini…

[SDV.GEN]Life Sciences [q-bio]/GeneticsSyndromes oro-facio-digitauxSéquençage haut-débitOral-facial-digital syndromesWhole-exome sequencingCiliopathyGenetics[SDV.GEN] Life Sciences [q-bio]/GeneticsGénétique[ SDV.GEN ] Life Sciences [q-bio]/GeneticsCiliopathies
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