• Title of article

    Congenital adrenal hyperplasias

  • Author/Authors

    Perrin C. White، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2001
  • Pages
    25
  • From page
    17
  • To page
    41
  • Abstract
    Congenital adrenal hyperplasia syndromes result from deficiencies of enzymes involved in corticosteroid biosynthesis. Most commonly, they are due to mutations in 21-hydroxylase. This chapter describes the clinical diagnosis and management of congenital adrenal hyperplasias throughout life, including in the fetus, child and adult. These clinical recommendations are explained in the context of the molecular and biochemical characteristics of the diseases.
  • Keywords
    congenital , adrenal hyperplasia , Androgens , Aldosterone , hydrocortisone , Cytochrome P-450 , Metabolism , steroid 21-monooxygenase , inborn errors , sex di?erentiation disorders , virilism , HLA antigens.
  • Journal title
    Best Practice and Research Clinical Endocrinology and Metabolism
  • Serial Year
    2001
  • Journal title
    Best Practice and Research Clinical Endocrinology and Metabolism
  • Record number

    465807

    • Link To Document
    https://search.isc.ac/dl/search/defaultta.aspx?DTC=10&DC=465807