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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.
Afiliação
  • Uddin KMF; Holy Family Red Crescent Medical College Dhaka Bangladesh.
  • Amin R; NeuroGen Technologies Ltd. Dhaka Bangladesh.
  • Majumder SN; Department of Medicine Dhaka Medical College Dhaka Bangladesh.
  • Aleem MA; Department of Medicine Dhaka Medical College Dhaka Bangladesh.
  • Rahaman A; International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR,B) Dhaka Bangladesh.
  • Dity NJ; NeuroGen Technologies Ltd. Dhaka Bangladesh.
  • Baqui MDA; NeuroGen Technologies Ltd. Dhaka Bangladesh.
  • Akter H; Holy Family Red Crescent Medical College Dhaka Bangladesh.
  • Rahman MM; NeuroGen Technologies Ltd. Dhaka Bangladesh.
  • Woodbury-Smith M; NeuroGen Technologies Ltd. Dhaka Bangladesh.
  • Scherer S; Department of Pediatrics Bangabandhu Sheikh Mujib Medical University (BSMMU) Dhaka Bangladesh.
  • Uddin M; Institute of Neuroscience Newcastle University Newcastle upon Tyne UK.
Clin Case Rep ; 6(8): 1426-1430, 2018 Aug.
Article em En | MEDLINE | ID: mdl-30147876
ABSTRACT
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2018 Tipo de documento: Article