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diagnosis management 21ohd acquired cap community cop cryptogenic endocrinology genetics organizing pathophysiology pediatrics
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 ... endocrinology #peds
Community Acquired Pneumonia (CAP) - Diagnosis and Management Pneumonia Signs/Symptoms: • Confusion/disorientation (LR + 1.9) • Cough
Community Acquired Pneumonia ... Signs/Symptoms: ... procalcitonin level Treatment ... Diagnosis #Management #treatment ... #Pulmonary #Community
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Males=Females SIGNS ... /SYMPTOMS: • Acute ... identified (autoimmune, meds ... , neoplastic) TREATMENT ... diagnosis #management #pulmonary
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