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diagnosis 21hydroxylasedeficiency algorithm anaphylaxis cardiology chf criteria criticalcare differential foamed genetics heartfailure icu management peds pharmacology symptoms 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
Clinical manifestations of anaphylaxis. Neurological (<15%): Dizziness, syncope, seizures, Confusion, impending doom. headache Angioedema: Lips, tongue, orbit,
Clinical manifestations ... arrest, Kounis syndrome ... Scrotal edema, uterine ... cramps, vaginal bleeding ... #anaphylaxis #signs
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 ... causing hypovolemia needing ... acute coronary syndrome
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