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21hydroxylasedeficiency diagnosis frozenshoulder genetics msk pediatrics peds signs stages staging symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
, vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Adhesive Capsulitis (Frozen Shoulder) - Pathogenesis and Clinical Findings • Primary (Idiopathic): Unknown etiology, but associated
autoimmune disorders (diabetes ... Increase => Months later ... tissue => Years later ... scapulothoracic) #AdhesiveCapsulitis ... FrozenShoulder #pathophysiology
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