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diagnosis 21hydroxylasedeficiency cardiology chf cold comparison criticalcare differential endocrinology foamed genetics heartfailure management pathophysiology pediatrics peds pharmacology rheumatology treatment urticaria
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD
Cold Urticaria Prevalence - 0.05% in the population Disease onset - Mostly 2nd to 4th decades of life Causes
decades of life Causes ... and clinical associations ... , Hypotension, shock ... Diagnostic tests - Ice ... rheumatology #comparison #table
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
essentially Cardiogenic Shock ... the determined cause ... #differential #algorithm ... cardiology #treatment #table ... #criticalcare #icu
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