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21hydroxylasedeficiency 21ohd cop diagnosis endocrinology genetics management organizing pathophysiology pneumonia pulmonary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
occur in utero as ... Signs/Symptoms/Complications ... Labia major & minor ... endocrinology #peds ... #pediatrics
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Cryptogenic Organizing ... Males=Females SIGNS ... usually misdiagnosed as ... CAP • Symptoms ... , neoplastic) TREATMENT
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