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Confirming the recessive inheritance of SCN1B mutations in develo | 49609

Journal of Neurology & Neurophysiology

ISSN - 2155-9562

Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy

15th EUROPEAN NEUROLOGY CONGRESS

August 29-31, 2017 | London, UK

Wafaa Ramadan, Nisha Patel, Shamsa Anazi, Amal Y Kentab, Fahad A Bashiri, Muddathir H Hamad, Lamya Jad, Mustafa A Salih, Hessa Alsaif, Mais Hashem, Eissa Faqeih, Hanan E Shamseddin and Fowzan S Alkuraya

King Faisal Specialist Hospital and Research Center, Saudi Arabia
King Saud University, Saudi Arabia
King Fahad Medical City, Saudi Arabia
Alfaisal University, Saudi Arabia

Posters & Accepted Abstracts: J Neurol Neurophysiol

Abstract :

Dominant SCN1B (Sodium channel subunit beta-1) mutations are known to cause several epilepsy syndromes in humans. Only two epilepsy patients to date have been reported to have recessive mutations in SCN1B as the likely cause of their phenotype. Here, we confirm the recessive inheritance of two novel SCN1B mutations in five children from three families with developmental epileptic encephalopathy. The ├ó┬?┬?negative├ó┬?┬Ł clinical exome in one of these families highlight the need to consider recessive mutations in the interpretation of variants in typically dominant genes.

Biography :

Wafaa Ramadan has completed her MBBS this June from AlFaisal University, Riyadh, KSA.

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