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21hydroxylasedeficiency clinical elbow endocrinology fracture genetics head hemarthrosis radial 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 ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics
Radial Head Elbow Fracture with displaced Fat Pads Intra-Articular Fracture of the Elbow with displaced fat pads
radiograph as dark streaks ... So even in a case ... called the “Sail sign ... trauma #clinical #radiology ... #msk #hemarthrosis
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