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Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME): Probable first family from India

Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME) is an extremely rare syndrome characterized by familial occurrence of postural and action-induced tremors of the hands but showing electrophysiologic findings of cortical reflex myoclonus. Patients also have cognitive decline and to...

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Autores principales: Sharma, Chandra Mohan, Nath, Kunal, Kumawat, Bansi Lal, Khandelwal, Dinesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4251019/
https://www.ncbi.nlm.nih.gov/pubmed/25506167
http://dx.doi.org/10.4103/0972-2327.144025
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author Sharma, Chandra Mohan
Nath, Kunal
Kumawat, Bansi Lal
Khandelwal, Dinesh
author_facet Sharma, Chandra Mohan
Nath, Kunal
Kumawat, Bansi Lal
Khandelwal, Dinesh
author_sort Sharma, Chandra Mohan
collection PubMed
description Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME) is an extremely rare syndrome characterized by familial occurrence of postural and action-induced tremors of the hands but showing electrophysiologic findings of cortical reflex myoclonus. Patients also have cognitive decline and tonic-clonic seizures, often precipitated by sleep deprivation or photic stimulation. We describe probably the first family from India of this ill-defined syndrome.
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spelling pubmed-42510192014-12-12 Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME): Probable first family from India Sharma, Chandra Mohan Nath, Kunal Kumawat, Bansi Lal Khandelwal, Dinesh Ann Indian Acad Neurol Case Report Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME) is an extremely rare syndrome characterized by familial occurrence of postural and action-induced tremors of the hands but showing electrophysiologic findings of cortical reflex myoclonus. Patients also have cognitive decline and tonic-clonic seizures, often precipitated by sleep deprivation or photic stimulation. We describe probably the first family from India of this ill-defined syndrome. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4251019/ /pubmed/25506167 http://dx.doi.org/10.4103/0972-2327.144025 Text en Copyright: © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sharma, Chandra Mohan
Nath, Kunal
Kumawat, Bansi Lal
Khandelwal, Dinesh
Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME): Probable first family from India
title Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME): Probable first family from India
title_full Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME): Probable first family from India
title_fullStr Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME): Probable first family from India
title_full_unstemmed Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME): Probable first family from India
title_short Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME): Probable first family from India
title_sort autosomal dominant cortical tremor, myoclonus, and epilepsy (adcme): probable first family from india
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4251019/
https://www.ncbi.nlm.nih.gov/pubmed/25506167
http://dx.doi.org/10.4103/0972-2327.144025
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