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A Newborn Falsely Suspected of Congenital Hypothyroidism due to Mutated Thyroxine-Binding Globulin with Low Binding Affinity.
Hengeveld, Rutger C C; Albersen, Monique; Hadders, Michael A H; Hellinga, Ilse; Bikker, Hennie; Heijboer, Annemieke C; Paul van Trotsenburg, A S; Hillebrand, Jacquelien J; Boelen, Anita; Zwaveling-Soonawala, Nitash.
Afiliação
  • Hengeveld RCC; Department of Clinical Chemistry, Amsterdam UMC, Central Diagnostic Laboratory, University of Amsterdam, Amsterdam, The Netherlands.
  • Albersen M; Department of Clinical Chemistry, Amsterdam UMC, Endocrine Laboratory, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Hadders MAH; Department of Molecular Cancer Research, Oncode Institute, University Medical Center Utrecht, Center for Molecular Medicine, Utrecht, The Netherlands.
  • Hellinga I; Department of Pediatric Endocrinology, Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands.
  • Bikker H; Department of Clinical Genetics, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Heijboer AC; Department of Clinical Chemistry, Amsterdam UMC, Central Diagnostic Laboratory, University of Amsterdam, Amsterdam, The Netherlands.
  • Paul van Trotsenburg AS; Department of Clinical Chemistry, Amsterdam UMC, Endocrine Laboratory, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Hillebrand JJ; Department of Pediatric Endocrinology, Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands.
  • Boelen A; Department of Clinical Chemistry, Amsterdam UMC, Central Diagnostic Laboratory, University of Amsterdam, Amsterdam, The Netherlands.
  • Zwaveling-Soonawala N; Department of Clinical Chemistry, Amsterdam UMC, Endocrine Laboratory, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Horm Res Paediatr ; 94(1-2): 76-80, 2021.
Article em En | MEDLINE | ID: mdl-34126618
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mutação de Sentido Incorreto / Hipotireoidismo Congênito / Doenças Genéticas Ligadas ao Cromossomo X / Globulina de Ligação a Tiroxina Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mutação de Sentido Incorreto / Hipotireoidismo Congênito / Doenças Genéticas Ligadas ao Cromossomo X / Globulina de Ligação a Tiroxina Idioma: En Ano de publicação: 2021 Tipo de documento: Article