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diagnosis 21hydroxylasedeficiency abnormal celiac endocrinology gastroenterology genetics hepatology lfts liver pathophysiology pediatrics peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
coding for the enzyme ... Signs/Symptoms/Complications ... : • Hyperkalemia ... Labia major & minor ... #21HydroxylaseDeficiency #21OHD
Suspected Celiac Disease - Diagnosis Algorithm Celiac disease suspected: • Signs and symptoms of celiac disease •
- Diagnosis Algorithm ... suspected: • Signs ... and symptoms of ... Elevated liver enzymes ... microscopic colitis Differential
Abnormal liver function tests algorithm. This figure details the initial response to abnormal liver blood tests.
function tests algorithm ... suspicious clinical symptoms ... /signs should be ... the magnitude of enzyme ... #Differential #
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