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diagnosis 21hydroxylasedeficiency 21ohd causes complications cushings diabetes diabeticketoacidosis differential dka genetics hypercortisolism hypertension indications pediatrics psychiatry secondary syndrome
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 ... #peds #pediatrics
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
Hypertension - Workup ... hypokalemia and metabolic ... bruit or signs ... Vasculitis • Endocrinologic ... Hypothyroidism, Primary
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
patient has good renal ... Due to neuronal metabolism ... Signs/Symptoms/Complications ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
Cushing's Syndrome - Hypercortisolism - Diagnosis and Clinical Features 1) Skin • Thin, easily bruisable skin with
not a feature of primary ... Endocrine and metabolic ... Imaging: 1) Primary ... Hypercortisolism #Diagnosis #signs ... #symptoms #endocrinology
Bulimia Nervosa: Complications GASTROINTESTINAL • Dehydration & inability to digest food -> Constipation • Recurrent vomiting exposes
/Osteoporosis RENAL ... Cardiac Arrest #BulimiaNervosa ... Complications #pathophysiology ... #diagnosis #signs ... #symptoms #psychiatry
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