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diagnosis 21hydroxylasedeficiency 21ohd adrenal genetics hyperuricemia insufficiency pathophysiology pediatrics uricacid
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... wasting crisis & hyperkalemia ... Complications: • Hyperkalemia ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Adrenal Insufficiency Differential Diagnosis Algorithm Clinical suspicion: Weakness, fatigue, nausea, musculoskeletal pain, dizziness, volume depletion, abdominal pain,
Insufficiency Differential ... Diagnosis Algorithm ... Weakness, fatigue, nausea ... hyponatremia, hyperkalemia ... #endocrinology
Hyperuricemia - Differential Diagnosis Algorithm Primary - Over-production • Increased turnover of nucleotides Primary
Diagnosis Algorithm ... Sarcoidosis • Hypercalcemia ... • Alcohol #gout ... #endocrinology ... #causes
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