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diagnosis differential pediatrics peds secondary 21hydroxylasedeficiency 21ohd brue chronic constipation event fatigue genetics geriatrics gout hypertension hyperuricemia indications lifethreatening neurology
Causes of Hypercalcemia - Differential Diagnosis Algorithm • Primary Hyperparathyroidism • Possible Familial Hypocalciuric Hypercalcemia
Causes of Hypercalcemia ... Differential Diagnosis Algorithm ... Granulomatous Disorders ... Differential #Diagnosis #Algorithm ... #Causes #endocrinology
Causes of Secondary / Provoked Seizures - Differential Diagnosis Algorithm Febrile Infection • Sepsis • Encephalitis • Meningitis Metabolic
Causes of Secondary ... Differential Diagnosis Algorithm ... • Meningitis Metabolic ... Hyperglycemia • Hypocalcemia ... #Causes
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Threatening Event (ALTE ... Myocarditis Metabolic ... Neuromuscular • Disorders ... #Causes #Peds #
Causes of Hypercalcemia Parathyroid gland structure-related • Primary hyperparathyroidism • Parathyroid adenoma • Parathyroid hyperplasia • Parathyroid
Causes of Hypercalcemia ... hypocalciuric hypercalcemia ... Vitamin D metabolic ... disorders • Excessive ... #Causes #endocrinology
Hyperuricemia - Differential Diagnosis Algorithm Primary - Over-production • Increased turnover of nucleotides Primary
Differential Diagnosis Algorithm ... Lymphoproliferative Disorders ... Sarcoidosis • Hypercalcemia ... #endocrinology ... #causes
Causes of Fatigue - Differential Diagnosis Algorithm Endocrine • Hypo/Hyperthyroidism • Diabetes • Pituitary Insufficiency • Adrenal
Causes of Fatigue ... Insufficiency Metabolic ... Liver Failure • Hypercalcemia ... • Somatization Disorder ... #causes
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... Short Stature (Late ... CHF) • Inborn Metabolism ... #endocrinology ... #causes #pediatrics
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 ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
with electrolyte disorders ... hypokalemia and metabolic ... Vasculitis • Endocrinologic ... Hyperthyroidism, Hypercalcemia ... Neurologic disorders
Pathogenesis of Select Causes of Constipation in Adults and in Elderly • Mechanical (ex. Bowel Obstruction,
Pathogenesis of Select Causes ... bowel contents • Metabolic ... Hypercalcemia) - ... neuromuscular disorders ... #constipation #pathophysiology
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