The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21hydroxylasedeficiency causes diagnosis femur fractures genetics msk pediatrics peds subtrochanteric
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Subtrochanteric Femur Fracture: Pathogenesis and clinical findings • Subtrochanteric region spans 5 cm distally from the
Fractures #msk #orthopedics ... #diagnosis #differential ... #causes #pathophysiology
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