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21hydroxylasedeficiency complications diabetes diabeticketoacidosis diagnosis dka genetics pediatrics peds psychiatry signs symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
To prevent hypokalemia ... patient has good renal ... Signs/Symptoms/Complications ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
Bulimia Nervosa: Complications GASTROINTESTINAL • Dehydration & inability to digest food -> Constipation • Recurrent vomiting exposes
/Osteoporosis RENAL ... ) • Overall: hypokalemia ... Cardiac Arrest #BulimiaNervosa ... Complications #pathophysiology ... #diagnosis #signs
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