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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Detalles Bibliográficos
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:
Case Reports
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
Descripción
Sumario: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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