Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree

Atypical manifestation of Huntington's disease (HD) could inform ongoing research into HD genetic modifiers not present in the primarily European populations studied to date. This work demonstrates that expanding HD genetic testing into under‐resourced healthcare settings can benefit both local...

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Autores principales: Al‐Mamun, Md Mahfuz, Sarker, Suprovath Kumar, Qadri, Syeda Kashfi, Shirin, Tahmina, Mohammad, Quazi Deen, LaRocque, Regina, Karlsson, Elinor K., Saha, Narayan, Asaduzzaman, Muhammad, Qadri, Firdausi, Mannoor, Md Kaiissar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134195/
https://www.ncbi.nlm.nih.gov/pubmed/27980761
http://dx.doi.org/10.1002/ccr3.743
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author Al‐Mamun, Md Mahfuz
Sarker, Suprovath Kumar
Qadri, Syeda Kashfi
Shirin, Tahmina
Mohammad, Quazi Deen
LaRocque, Regina
Karlsson, Elinor K.
Saha, Narayan
Asaduzzaman, Muhammad
Qadri, Firdausi
Mannoor, Md Kaiissar
author_facet Al‐Mamun, Md Mahfuz
Sarker, Suprovath Kumar
Qadri, Syeda Kashfi
Shirin, Tahmina
Mohammad, Quazi Deen
LaRocque, Regina
Karlsson, Elinor K.
Saha, Narayan
Asaduzzaman, Muhammad
Qadri, Firdausi
Mannoor, Md Kaiissar
author_sort Al‐Mamun, Md Mahfuz
collection PubMed
description Atypical manifestation of Huntington's disease (HD) could inform ongoing research into HD genetic modifiers not present in the primarily European populations studied to date. This work demonstrates that expanding HD genetic testing into under‐resourced healthcare settings can benefit both local communities and ongoing research into HD etiology and new therapies.
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spelling pubmed-51341952016-12-15 Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree Al‐Mamun, Md Mahfuz Sarker, Suprovath Kumar Qadri, Syeda Kashfi Shirin, Tahmina Mohammad, Quazi Deen LaRocque, Regina Karlsson, Elinor K. Saha, Narayan Asaduzzaman, Muhammad Qadri, Firdausi Mannoor, Md Kaiissar Clin Case Rep Case Reports Atypical manifestation of Huntington's disease (HD) could inform ongoing research into HD genetic modifiers not present in the primarily European populations studied to date. This work demonstrates that expanding HD genetic testing into under‐resourced healthcare settings can benefit both local communities and ongoing research into HD etiology and new therapies. John Wiley and Sons Inc. 2016-11-11 /pmc/articles/PMC5134195/ /pubmed/27980761 http://dx.doi.org/10.1002/ccr3.743 Text en © 2016 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Al‐Mamun, Md Mahfuz
Sarker, Suprovath Kumar
Qadri, Syeda Kashfi
Shirin, Tahmina
Mohammad, Quazi Deen
LaRocque, Regina
Karlsson, Elinor K.
Saha, Narayan
Asaduzzaman, Muhammad
Qadri, Firdausi
Mannoor, Md Kaiissar
Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree
title Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree
title_full Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree
title_fullStr Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree
title_full_unstemmed Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree
title_short Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree
title_sort examination of huntington's disease with atypical clinical features in a bangladeshi family tree
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134195/
https://www.ncbi.nlm.nih.gov/pubmed/27980761
http://dx.doi.org/10.1002/ccr3.743
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