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21hydroxylasedeficiency adhesivecapsulitis diagnosis endocrinology genetics pediatrics peds signs stages staging
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Adhesive Capsulitis (Frozen Shoulder) - Pathogenesis and Clinical Findings • Primary (Idiopathic): Unknown etiology, but associated
Pathogenesis and Clinical ... AdhesiveCapsulitis #FrozenShoulder ... #pathophysiology ... #diagnosis #symptoms ... stages #staging #msk
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