Epilepsy associated tuberous sclerosis; a case report from Bangladesh

Tuberous sclerosis or Bourneville's disease is a rare autosomal dominant disease affecting many organs like the brain, heart, lungs, eyes, kidneys and skin. It is characterized by neurological manifestation like epilepsy, cutaneous changes and the formation of benign lesions in multiple organs....

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Detalles Bibliográficos
Autores principales: Shrestha, Abhigan Babu, Shrestha, Sajina, Seemanta, Senjuti, Pokharel, Pashupati, Alam, Waqar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118511/
https://www.ncbi.nlm.nih.gov/pubmed/35600170
http://dx.doi.org/10.1016/j.amsu.2022.103738
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author Shrestha, Abhigan Babu
Shrestha, Sajina
Seemanta, Senjuti
Pokharel, Pashupati
Alam, Waqar
author_facet Shrestha, Abhigan Babu
Shrestha, Sajina
Seemanta, Senjuti
Pokharel, Pashupati
Alam, Waqar
author_sort Shrestha, Abhigan Babu
collection PubMed
description Tuberous sclerosis or Bourneville's disease is a rare autosomal dominant disease affecting many organs like the brain, heart, lungs, eyes, kidneys and skin. It is characterized by neurological manifestation like epilepsy, cutaneous changes and the formation of benign lesions in multiple organs. The symptoms are apparent only in late childhood, which limits the early diagnosis in infancy. Here, we report a case of a 15 year old female child with tuberous sclerosis.
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spelling pubmed-91185112022-05-20 Epilepsy associated tuberous sclerosis; a case report from Bangladesh Shrestha, Abhigan Babu Shrestha, Sajina Seemanta, Senjuti Pokharel, Pashupati Alam, Waqar Ann Med Surg (Lond) Case Report Tuberous sclerosis or Bourneville's disease is a rare autosomal dominant disease affecting many organs like the brain, heart, lungs, eyes, kidneys and skin. It is characterized by neurological manifestation like epilepsy, cutaneous changes and the formation of benign lesions in multiple organs. The symptoms are apparent only in late childhood, which limits the early diagnosis in infancy. Here, we report a case of a 15 year old female child with tuberous sclerosis. Elsevier 2022-05-11 /pmc/articles/PMC9118511/ /pubmed/35600170 http://dx.doi.org/10.1016/j.amsu.2022.103738 Text en © 2022 The Authors. Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Shrestha, Abhigan Babu
Shrestha, Sajina
Seemanta, Senjuti
Pokharel, Pashupati
Alam, Waqar
Epilepsy associated tuberous sclerosis; a case report from Bangladesh
title Epilepsy associated tuberous sclerosis; a case report from Bangladesh
title_full Epilepsy associated tuberous sclerosis; a case report from Bangladesh
title_fullStr Epilepsy associated tuberous sclerosis; a case report from Bangladesh
title_full_unstemmed Epilepsy associated tuberous sclerosis; a case report from Bangladesh
title_short Epilepsy associated tuberous sclerosis; a case report from Bangladesh
title_sort epilepsy associated tuberous sclerosis; a case report from bangladesh
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118511/
https://www.ncbi.nlm.nih.gov/pubmed/35600170
http://dx.doi.org/10.1016/j.amsu.2022.103738
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