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21ohd diagnosis fistula genetics management pathophysiology pediatrics peds summary vascular
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... a scrotum #21HydroxylaseDeficiency ... pathophysiology #genetics #endocrinology
Aortoenteric Fistula - Diagnosis and Management Summary Epidemiology: • Uncommon but life-threatening • Most common site of bowel connection
Aortoenteric Fistula ... duodenum Clinical Signs ... /Symptoms: • Classic ... patients with acute ... Residency @CMC_IM #Aortoenteric
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