Kv7.2 (KCNQ2) channel dysfunctions cause a rare form of neonatal and infantile epileptic and developmental encephalopathy (MIM 613720).1 Unlike early clinical features and the epilepsy phenotype of KCNQ2 encephalopathy, data about the long-term developmental outcome are lacking. We followed up for over 3 decades a girl with this disease

KCNQ2 encephalopathy manifesting with Rett-like features A follow-up into adulthood / Mastrangelo, Mario; Manti, Filippo; Giannini, Maria Teresa; Guerrini, Renzo; Leuzzi, Vincenzo. - In: NEUROLOGY. GENETICS. - ISSN 2376-7839. - (2020). [10.1212/NXG.0000000000000510]

KCNQ2 encephalopathy manifesting with Rett-like features A follow-up into adulthood

Mario Mastrangelo
Primo
Writing – Original Draft Preparation
;
Filippo Manti
Secondo
Writing – Original Draft Preparation
;
Maria Teresa Giannini
Writing – Review & Editing
;
Vincenzo Leuzzi
Ultimo
Writing – Review & Editing
2020

Abstract

Kv7.2 (KCNQ2) channel dysfunctions cause a rare form of neonatal and infantile epileptic and developmental encephalopathy (MIM 613720).1 Unlike early clinical features and the epilepsy phenotype of KCNQ2 encephalopathy, data about the long-term developmental outcome are lacking. We followed up for over 3 decades a girl with this disease
2020
KCNQ2; Encephalopathy, Intellectual Disability
01 Pubblicazione su rivista::01a Articolo in rivista
KCNQ2 encephalopathy manifesting with Rett-like features A follow-up into adulthood / Mastrangelo, Mario; Manti, Filippo; Giannini, Maria Teresa; Guerrini, Renzo; Leuzzi, Vincenzo. - In: NEUROLOGY. GENETICS. - ISSN 2376-7839. - (2020). [10.1212/NXG.0000000000000510]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1437079
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