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Longitudinal serum and urine steroid metabolite profiling in a 46,XY infant with prenatally identified POR deficiency.
Ono, Hiroyuki; Numakura, Chikahiko; Homma, Keiko; Hasegawa, Tomonobu; Tsutsumi, Seiji; Kato, Fumiko; Fujisawa, Yasuko; Fukami, Maki; Ogata, Tsutomu.
Afiliação
  • Ono H; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Numakura C; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan.
  • Homma K; Clinical Laboratory, Keio University Hospital, Tokyo, Japan.
  • Hasegawa T; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
  • Tsutsumi S; Department of Obstetrics and Gynecology, Yamagata University School of Medicine, Yamagata, Japan.
  • Kato F; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Fujisawa Y; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Fukami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
  • Ogata T; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan. Electronic address: tomogata@hama-med.ac.jp.
J Steroid Biochem Mol Biol ; 178: 177-184, 2018 04.
Article em En | MEDLINE | ID: mdl-29289577
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esteroides / Esteroide 17-alfa-Hidroxilase / Fenótipo de Síndrome de Antley-Bixler / Transtorno 46,XY do Desenvolvimento Sexual / Doenças Fetais Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esteroides / Esteroide 17-alfa-Hidroxilase / Fenótipo de Síndrome de Antley-Bixler / Transtorno 46,XY do Desenvolvimento Sexual / Doenças Fetais Idioma: En Ano de publicação: 2018 Tipo de documento: Article