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Case of H syndrome with massive skin involvement, retroperitoneal fibrosis and Raynaud's phenomenon with a novel mutation in the SLC29A3 gene.
Fujita, Etsuko; Komine, Mayumi; Tsuda, Hidetoshi; Adachi, Akimasa; Murata, Satoru; Kamata, Yasuyuki; Minota, Seiji; Ohtsuki, Mamitaro.
Afiliação
  • Fujita E; Department of Dermatology, Jichi Medical University, Shimotsuke, Japan.
  • Komine M; Department of Dermatology, Jichi Medical University, Shimotsuke, Japan.
  • Tsuda H; Department of Dermatology, Jichi Medical University, Shimotsuke, Japan.
  • Adachi A; Department of Dermatology, Jichi Medical University, Shimotsuke, Japan.
  • Murata S; Department of Dermatology, Jichi Medical University, Shimotsuke, Japan.
  • Kamata Y; Department of Allergy & Rheumatology, Jichi Medical University, Shimotsuke, Japan.
  • Minota S; Department of Allergy & Rheumatology, Jichi Medical University, Shimotsuke, Japan.
  • Ohtsuki M; Department of Dermatology, Jichi Medical University, Shimotsuke, Japan.
J Dermatol ; 42(12): 1169-71, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26074390
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Raynaud / Fibrose Retroperitoneal / Dermatopatias Genéticas / Histiocitose / Contratura / Proteínas de Transporte de Nucleosídeos / Perda Auditiva Neurossensorial Tipo de estudo: Prognostic_studies Limite: Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Raynaud / Fibrose Retroperitoneal / Dermatopatias Genéticas / Histiocitose / Contratura / Proteínas de Transporte de Nucleosídeos / Perda Auditiva Neurossensorial Tipo de estudo: Prognostic_studies Limite: Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article