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Research Article| Volume 7, ISSUE 1, P43-56, January 1991

Myxedema Coma

  • Author Footnotes
    * Teaching Fellow
    Lyle Myers
    Correspondence
    Address reprint requests to: LCDR Lyle Myers, MD MC, USNR, Division of Endocrinology-Metabolism, Department of Internal Medicine, National Naval Medical Center, Bethesda, MD 20889-5000
    Footnotes
    * Teaching Fellow
    Affiliations
    From the Division of Endocrinology-Metabolism, Department of Internal Medicine, National Naval Medical Center, and the Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland
    Search for articles by this author
  • Author Footnotes
    † Assistant Professor
    James Hays
    Footnotes
    † Assistant Professor
    Affiliations
    From the Division of Endocrinology-Metabolism, Department of Internal Medicine, National Naval Medical Center, and the Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland
    Search for articles by this author
  • Author Footnotes
    * Teaching Fellow
    † Assistant Professor
      This paper is only available as a PDF. To read, Please Download here.
      Myxedema coma was described during the nineteenth century, but, despite the availability of specific hormonal therapy, the mortality rate remains high. This article discusses the causes, pathophysiology, and clinical presentation of myxedema coma. The differentiation of myxedema coma from the euthyroid sick syndromes is examined. General supportive care as well as specific hormonal replacement therapy is addressed.
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