Apparent Cortisone Reductase Deficiency: A Rare Cause of Hyperandrogenemia and Hypercortisolism

    January 2000 in “ Hormone Research in Paediatrics ”
    Anna Biason‐Lauber, Stephan L. Suter, Cedric Shackleton, M. Zachmann
    Studysummary In this case study, a 55-year-old woman with androgenetic alopecia was ultimately diagnosed with hepatic cortisone reductase deficiency after initially suspected 21-hydroxylase deficiency was ruled out.
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