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21hydroxylasedeficiency 21ohd diagnosis endocrinology fracture localization orthopedics pathophysiology pediatrics peds spinal spine trauma
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... scrotum & enlarged penis ... may look like a penis ... pathophysiology #genetics
Orthopedic Essentials - Spinal Trauma and Spine Classification DENIS THREE COLUMN CONCEPT Anterior column:
DENIS THREE COLUMN ... Facet capsule DENIS ... fractures: Don't cause ... compromisation > 1/3 • Bilateral ... • According to Denis
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