2 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical Findings ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
Some exam findings ... essentially Cardiogenic Shock ... algorithm #management #cardiology ... treatment #table #foamed ... #heartfailure #