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cop cryptogenic endocrinology genetics management organizing pathophysiology pediatrics pulmonary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology ... endocrinology #peds
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
decade of life, Males ... =Females SIGNS/ ... SYMPTOMS: • Acute ... misdiagnosed as CAP • Symptoms ... identified (autoimmune, meds
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