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21ohd genetics lichen nejm pediatrics planus striae wickhams
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... , vomiting • Late ... #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Lichen Planus- ...On examination, numerous purple papules were noted on the anterior surface of the forearms
sawtooth rete pegs ... treated, and the later ... #NEJM #clinical ... #photo #lichen # ... planus #derm #wickhams
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