Patient with Dravet syndrome: A case report

Dravet syndrome is rare genetic epilepsy syndrome and epileptic encephalopathy. The patient initially has normal developmental profile with plateau or regression that begins after seizure onset. We report a case of two‐year‐old child diagnosed as dravet syndrome with moderate cerebral atrophy and ve...

Descripción completa

Detalles Bibliográficos
Autores principales: Yadav, Rukesh, Shah, Sangam, Bhandari, Bibek, Marasini, Kundan, Mandal, Prince, Murarka, Hritik, Pandey, Anuj Kumar, Sharma Paudel, Basanta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069364/
https://www.ncbi.nlm.nih.gov/pubmed/35540719
http://dx.doi.org/10.1002/ccr3.5840
_version_ 1784700414086610944
author Yadav, Rukesh
Shah, Sangam
Bhandari, Bibek
Marasini, Kundan
Mandal, Prince
Murarka, Hritik
Pandey, Anuj Kumar
Sharma Paudel, Basanta
author_facet Yadav, Rukesh
Shah, Sangam
Bhandari, Bibek
Marasini, Kundan
Mandal, Prince
Murarka, Hritik
Pandey, Anuj Kumar
Sharma Paudel, Basanta
author_sort Yadav, Rukesh
collection PubMed
description Dravet syndrome is rare genetic epilepsy syndrome and epileptic encephalopathy. The patient initially has normal developmental profile with plateau or regression that begins after seizure onset. We report a case of two‐year‐old child diagnosed as dravet syndrome with moderate cerebral atrophy and ventricular dilatation as rare MRI finding.
format Online
Article
Text
id pubmed-9069364
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-90693642022-05-09 Patient with Dravet syndrome: A case report Yadav, Rukesh Shah, Sangam Bhandari, Bibek Marasini, Kundan Mandal, Prince Murarka, Hritik Pandey, Anuj Kumar Sharma Paudel, Basanta Clin Case Rep Case Reports Dravet syndrome is rare genetic epilepsy syndrome and epileptic encephalopathy. The patient initially has normal developmental profile with plateau or regression that begins after seizure onset. We report a case of two‐year‐old child diagnosed as dravet syndrome with moderate cerebral atrophy and ventricular dilatation as rare MRI finding. John Wiley and Sons Inc. 2022-05-05 /pmc/articles/PMC9069364/ /pubmed/35540719 http://dx.doi.org/10.1002/ccr3.5840 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Yadav, Rukesh
Shah, Sangam
Bhandari, Bibek
Marasini, Kundan
Mandal, Prince
Murarka, Hritik
Pandey, Anuj Kumar
Sharma Paudel, Basanta
Patient with Dravet syndrome: A case report
title Patient with Dravet syndrome: A case report
title_full Patient with Dravet syndrome: A case report
title_fullStr Patient with Dravet syndrome: A case report
title_full_unstemmed Patient with Dravet syndrome: A case report
title_short Patient with Dravet syndrome: A case report
title_sort patient with dravet syndrome: a case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069364/
https://www.ncbi.nlm.nih.gov/pubmed/35540719
http://dx.doi.org/10.1002/ccr3.5840
work_keys_str_mv AT yadavrukesh patientwithdravetsyndromeacasereport
AT shahsangam patientwithdravetsyndromeacasereport
AT bhandaribibek patientwithdravetsyndromeacasereport
AT marasinikundan patientwithdravetsyndromeacasereport
AT mandalprince patientwithdravetsyndromeacasereport
AT murarkahritik patientwithdravetsyndromeacasereport
AT pandeyanujkumar patientwithdravetsyndromeacasereport
AT sharmapaudelbasanta patientwithdravetsyndromeacasereport

Ejemplares similares