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21hydroxylasedeficiency 21ohd clincal derm genetics lichen palmare pediatrics planus striae striatum wickhams xanthoma
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Xanthoma Striatum Palmare- A 49-year-old man was referred to the metabolic clinic for evaluation of severe
the metabolic clinic ... evaluation of severe hypercholesterolemia ... life, making it difficult ... #NEJM #clincal # ... photo #xanthoma
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 #
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