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diagnosis 21hydroxylasedeficiency celiac endocrinology evaluation gastroenterology genetics hypomagnesemia magnesium management pathophysiology pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... Signs/Symptoms/Complications ... Labia major & minor ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Suspected Celiac Disease - Diagnosis Algorithm Celiac disease suspected: • Signs and symptoms of celiac disease •
- Diagnosis Algorithm ... suspected: • Signs ... and symptoms of ... • Iron-deficiency ... unresponsive to treatment
Clinical Feature of Hypomagnesemia and Magnesium Deficiency • Electrolyte Disturbance: Hypokalemia, Hypocalcemia • Neuromuscular and central
Electrolyte Disturbance: Hypokalemia ... , Hypocalcemia ... Atherosclerotic vascular disease ... Hypomagnesemia #diagnosis #signs ... #symptoms #Treatment
Evaluation and Management of Hypokalemia Hypokalemia is often asymptomatic. Evaluation begins with a search for warning signs
search for warning signs ... or symptoms warranting ... urgent treatment ... underlying heart disease ... #Evaluation #Algorithm
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