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An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)

Epidermodysplasia verruciformis (EV) is an extremely rare hereditary skin disease characterized by an abnormal susceptibility to the human papilloma virus (HPV) with an increased risk of cutaneous malignancy. Here we report the first female severe EV case in Bangladesh, a 10‐year‐old girl with a non...

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Autores principales: Uddin, K. M. Furkan, Amin, Robed, Majumder, Sabbiha Nadia, Aleem, Mohammad Abdul, Rahaman, Atikur, Dity, Nushrat Jahan, Baqui, M. D. Abdul, Akter, Hosneara, Rahman, Muhammad Mizanur, Woodbury‐Smith, Marc, Scherer, Stephen, Uddin, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099040/
https://www.ncbi.nlm.nih.gov/pubmed/30147876
http://dx.doi.org/10.1002/ccr3.1595
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author Uddin, K. M. Furkan
Amin, Robed
Majumder, Sabbiha Nadia
Aleem, Mohammad Abdul
Rahaman, Atikur
Dity, Nushrat Jahan
Baqui, M. D. Abdul
Akter, Hosneara
Rahman, Muhammad Mizanur
Woodbury‐Smith, Marc
Scherer, Stephen
Uddin, Mohammed
author_facet Uddin, K. M. Furkan
Amin, Robed
Majumder, Sabbiha Nadia
Aleem, Mohammad Abdul
Rahaman, Atikur
Dity, Nushrat Jahan
Baqui, M. D. Abdul
Akter, Hosneara
Rahman, Muhammad Mizanur
Woodbury‐Smith, Marc
Scherer, Stephen
Uddin, Mohammed
author_sort Uddin, K. M. Furkan
collection PubMed
description Epidermodysplasia verruciformis (EV) is an extremely rare hereditary skin disease characterized by an abnormal susceptibility to the human papilloma virus (HPV) with an increased risk of cutaneous malignancy. Here we report the first female severe EV case in Bangladesh, a 10‐year‐old girl with a nonsense somatic mutation impacting ANKRD26 gene.
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spelling pubmed-60990402018-08-24 An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome) Uddin, K. M. Furkan Amin, Robed Majumder, Sabbiha Nadia Aleem, Mohammad Abdul Rahaman, Atikur Dity, Nushrat Jahan Baqui, M. D. Abdul Akter, Hosneara Rahman, Muhammad Mizanur Woodbury‐Smith, Marc Scherer, Stephen Uddin, Mohammed Clin Case Rep Case Reports Epidermodysplasia verruciformis (EV) is an extremely rare hereditary skin disease characterized by an abnormal susceptibility to the human papilloma virus (HPV) with an increased risk of cutaneous malignancy. Here we report the first female severe EV case in Bangladesh, a 10‐year‐old girl with a nonsense somatic mutation impacting ANKRD26 gene. John Wiley and Sons Inc. 2018-06-05 /pmc/articles/PMC6099040/ /pubmed/30147876 http://dx.doi.org/10.1002/ccr3.1595 Text en © 2018 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://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
Uddin, K. M. Furkan
Amin, Robed
Majumder, Sabbiha Nadia
Aleem, Mohammad Abdul
Rahaman, Atikur
Dity, Nushrat Jahan
Baqui, M. D. Abdul
Akter, Hosneara
Rahman, Muhammad Mizanur
Woodbury‐Smith, Marc
Scherer, Stephen
Uddin, Mohammed
An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
title An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
title_full An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
title_fullStr An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
title_full_unstemmed An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
title_short An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
title_sort ankrd26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (tree man syndrome)
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099040/
https://www.ncbi.nlm.nih.gov/pubmed/30147876
http://dx.doi.org/10.1002/ccr3.1595
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