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diagnosis 21hydroxylasedeficiency 21ohd emesis endocrinology hypokalemia pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... loss, vomiting ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Pediatric Vomiting - Gastrointestinal and Systemic Causes - Differential Diagnosis Algorithm Hepatobiliary: • Acute Hepatitis • Acute
Pediatric Vomiting ... - Differential ... Diagnosis Algorithm ... • Uremia • Hypercalcemia ... #Causes #Peds #
Pragmatic diagnostic algorithm for hypokalemia. ***Typical presentations: • Vomiting: urine Na/Cl > 1.6, low urine
presentations: • Vomiting ... urine Na/Cl < 0.7, high ... confirmed via genetic ... #diagnosis #differential ... #algorithm #nephrology
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