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      One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study.

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          Abstract

          Congenital adrenal hyperplasia due to 21-hydroxylase deficiency results in cortisol and aldosterone deficiency and is, in its most severe form, lethal. We aimed to assess the effect of historical medical improvements in the care of patients with this disorder over time and to assess the effects of neonatal screening in Sweden.

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          Author and article information

          Journal
          Lancet Diabetes Endocrinol
          The lancet. Diabetes & endocrinology
          2213-8595
          2213-8587
          Sep 2013
          : 1
          : 1
          Affiliations
          [1 ] Department of Molecular Medicine and Surgery, Centre for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Obstetrics and Gynaecology, Karolinska University Hospital Huddinge, Stockholm, Sweden. Electronic address: sebastian.gidlof@karolinska.se.
          [2 ] Department of Molecular Medicine and Surgery, Centre for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Endocrinology, Metabolism and Diabetes, Karolinska University Hospital Solna, Stockholm, Sweden.
          [3 ] Department of Paediatrics, Jönköping Hospital, Jönköping, Sweden.
          [4 ] Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, Stockholm, Sweden.
          [5 ] Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
          [6 ] Department of Molecular Medicine and Surgery, Centre for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden; Centre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, Stockholm, Sweden.
          [7 ] Department of Molecular Medicine and Surgery, Centre for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden; Paediatric Endocrinology, Karolinska University Hospital Solna, Stockholm, Sweden.
          Article
          S2213-8587(13)70007-X
          10.1016/S2213-8587(13)70007-X
          24622265
          48084fa2-07cc-4c83-8990-479c0b26fa0b
          Copyright © 2013 Elsevier Ltd. All rights reserved.
          History

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