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diagnosis causes hypocalcemia pathophysiology peds 21hydroxylasedeficiency 21ohd cah congenitaladrenalhyperplasia genetics gout highcalcium hypertension hyperuricemia indications insufficiency lowcalcium pth secondary shortstature
Hypercalcemia - Differential Diagnosis Algorithm Primary Hyperparathyroidism • Adenoma • Hyperplasia • MEN 1 and 2A Tertiary Hyperparathyroidism
Differential Diagnosis ... Algorithm Primary ... #Differential # ... Diagnosis #Algorithm ... #Endocrinology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... #CAH #algorithm ... #causes #pediatrics ... CongenitalAdrenalHyperplasia #diagnosis #comparison ... treatment #Peds #Endocrinology
Hypercalcemia - Differential Diagnosis Algorithm Elevated PTH (High or normal): • Primary Hyperparathyroidism • Familial Hypocalciuric Hypercalcemia Low
Differential Diagnosis ... Algorithm Elevated ... Tumors: Lung, SCC, renal ... #Differential # ... #causes #endocrinology
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
Hypocalcemia - Differential ... Diagnosis Algorithm ... - Congenital (Pediatric ... • Chronic Renal ... #PTH #endocrinology
Adrenal Insufficiency Differential Diagnosis Algorithm Clinical suspicion: Weakness, fatigue, nausea, musculoskeletal pain, dizziness, volume depletion, abdominal pain,
Differential Diagnosis ... Algorithm Clinical ... hyponatremia, hyperkalemia ... #Diagnosis #Algorithm ... #endocrinology
Causes of Hypocalcemia - Differential Diagnosis Algorithm • Extravascular: Pancreatitis, surgery, acute phosphate intake and renal
Causes of Hypocalcemia ... - Differential ... phosphate intake and renal ... Gadolinium contrast agents ... #Differential #
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Short Stature - Differential ... Diagnosis Algorithm ... • Congenital Adrenal ... #endocrinology ... #causes #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... 21-OHD in the adrenal ... as "congenital adrenal ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Hyperuricemia - Differential Diagnosis Algorithm Primary - Over-production • Increased turnover of nucleotides Primary
Hyperuricemia - Differential ... Diagnosis Algorithm ... Sarcoidosis • Hypercalcemia ... #Diagnosis #Algorithm ... #endocrinology
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
Hypertension - Workup and Differential ... antihypertensive agents ... Vasculitis • Endocrinologic ... Hyperthyroidism, Hypercalcemia ... Workup #causes #Differential
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