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21hydroxylasedeficiency diagnosis fistula genetics management pediatrics peds summary vascular
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
, vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Aortoenteric Fistula - Diagnosis and Management Summary Epidemiology: • Uncommon but life-threatening • Most common site of bowel connection
Aortoenteric Fistula ... that precedes a later ... Pathophysiology: ... - CMC IM Residency ... @CMC_IM #Aortoenteric
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