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21hydroxylasedeficiency cardiology chf criticalcare diagnosis differential foamed genetics heartfailure icu management peds pharmacology table
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 ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
Signs of poor perfusion ... status and low urine ... Signs of congestion ... acute coronary syndrome ... #differential #algorithm
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