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21hydroxylasedeficiency bilateral blines cop cryptogenic diagnosis endocrinology genetics lung management organizing pathophysiology pediatrics pocus pulmonary ultrasound
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Bilateral B-Lines in case of Pneumonia on Lung POCUS Young healthy pt with fever/dyspnea. POCUS lung exam
travel hx, home meds ... Differential Bilat ... interstitial lung disease ... partially seen shred sign ... #Lung #POCUS #clinical
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 Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Males=Females SIGNS ... /SYMPTOMS: • Acute ... DIAGNOSTICS: Clinical ... identified (autoimmune, meds ... steroids for severe disease
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