We present a patient affected by Dravet syndrome. Thorough analysis of genes that might be involved in the pathogenesis of such phenotype with both conventional and next generation sequencing resulted negative, therefore she was investigated by a-GCH that showed the presence of an unbalanced translocation resulting in a der(4)t(4;8)(p16.3,p23.3). This was an unconventional translocation, different from the recurrent translocation affiliated with WHS and did not involve LETM1.

Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 gene

CICCONE, ROBERTO;
2013-01-01

Abstract

We present a patient affected by Dravet syndrome. Thorough analysis of genes that might be involved in the pathogenesis of such phenotype with both conventional and next generation sequencing resulted negative, therefore she was investigated by a-GCH that showed the presence of an unbalanced translocation resulting in a der(4)t(4;8)(p16.3,p23.3). This was an unconventional translocation, different from the recurrent translocation affiliated with WHS and did not involve LETM1.
2013
Esperti anonimi
Inglese
Internazionale
STAMPA
56
10
551
555
5
Der(4)t(4;8)(p16.3,p23.3); Dravet syndrome; WHS; Anticonvulsants; Calcium-Binding Proteins; Child; Chromosomes, Human, Pair 4; Epilepsies, Myoclonic; Female; Humans; Membrane Proteins; Phenotype; Translocation, Genetic; Treatment Outcome; Valproic Acid; Genetics; Genetics (clinical)
no
9
info:eu-repo/semantics/article
262
Bayindir, Baran; Piazza, Elena; Della Mina, Erika; Limongelli, Ivan; Brustia, Francesca; Ciccone, Roberto; Veggiotti, Pierangelo; Zuffardi, Orsetta; D...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1184862
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