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21hydroxylasedeficiency cardiology chf criticalcare diagnosis differential endocrinology foamed genetics heartfailure icu management pathophysiology pediatrics peds pharmacology treatment
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
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
Signs of congestion ... essentially Cardiogenic Shock ... the determined cause ... #differential #algorithm ... cardiology #treatment #table
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