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Unusual Proliferative Glomerulonephritis in a Patient Diagnosed to Have Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome with a Novel Mutation in the GATA3 Gene.
Kamezaki, Michitsugu; Kusaba, Tetsuro; Adachi, Takaomi; Yamashita, Noriyuki; Nakata, Mayumi; Ota, Noriyoshi; Shiotsu, Yayoi; Ishida, Mami; Usui, Takeshi; Tamagaki, Keiichi.
Afiliação
  • Kamezaki M; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
  • Kusaba T; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
  • Adachi T; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
  • Yamashita N; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
  • Nakata M; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
  • Ota N; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
  • Shiotsu Y; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
  • Ishida M; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
  • Usui T; Department of Medical Genetics, Shizuoka General Hospital, Japan.
  • Tamagaki K; Division of Nephrology, Department of Medicine, Kyoto Prefectural University of Medicine, Japan.
Intern Med ; 56(11): 1393-1397, 2017.
Article em En | MEDLINE | ID: mdl-28566604

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glomerulonefrite / Perda Auditiva Neurossensorial / Hipoparatireoidismo / Nefrose Tipo de estudo: Diagnostic_studies Limite: Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glomerulonefrite / Perda Auditiva Neurossensorial / Hipoparatireoidismo / Nefrose Tipo de estudo: Diagnostic_studies Limite: Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article