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21hydroxylasedeficiency diagnosis dialysis differential endocrinology genetics pathophysiology pediatrics peritoneal
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Peritoneal Dialysis Complications Peritonitis: • Can't miss! 6% of cases result in death • Diagnostics:
Peritoneal Dialysis Complications ... 6% of cases result ... Swimming, Presence of pets ... Always evaluate for constipation ... #nephrology #diagnosis
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