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diagnosis rheumatology 21hydroxylasedeficiency comparison disease gout management pediatrics peds pseudogout pyrophosphate
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
CPPD vs Gout == CPPD == Think About CPPD When: • Self-limited synovitis after surgery/trauma (> 65
CPPD vs Gout ... disease states Pathophysiology ... precipitates with calcium ... Monosodium urate deposition ... • Metabolic syndrome
Pseudogout Summary - Calcium Pyrophosphate Deposition Disease (CPPD) Pathophysiology: Pyrophosphate produced by chondrocytes likely precipitates with calcium to
Pseudogout Summary - Calcium ... Pyrophosphate Deposition ... Pathophysiology ... Crowned Dens Syndrome ... #Deposition #Disease
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