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21hydroxylasedeficiency cardiology constrictive genetics pathophysiology pericarditis pocus
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 ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Constrictive Pericarditis on Echocardiogram A 55-year-old female marathon runner presents to clinic w/ 6-months of worsening breathlessness
runner presents to clinic ... 100/82, HR 74, JVP ... ASA, Kussmaul's sign ... , marked pedal edema ... #a4c #pocus #clinical
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