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21hydroxylasedeficiency aortoenteric diagnosis endocrinology management pediatrics summary vascular
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 ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Aortoenteric Fistula - Diagnosis and Management Summary Epidemiology: • Uncommon but life-threatening • Most common site of bowel connection
Aortoenteric Fistula ... the duodenum Clinical ... Signs/Symptoms: ... • Should be on differential ... Pathophysiology:
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