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21hydroxylasedeficiency diagnosis genetics k management pediatrics peds potassium treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... 21-OHD in the adrenal ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Hyperkalemia - Diagnosis and Management - GrepMed Handbook S/Sx: Most pts asymptomatic. Weakness, cramping, nausea, paresthesias, palpitations,
Weakness, cramping, nausea ... , rhabdo/crush injury ... Cortisol+ACTH stim test ... only if no clear cause ... Treatment #potassium #nephrology
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