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pathophysiology 21ohd diagnosis endocrinology frozenshoulder genetics pediatrics peds stages staging
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 ... vomiting • Late (shock ... a scrotum #21HydroxylaseDeficiency
Adhesive Capsulitis (Frozen Shoulder) - Pathogenesis and Clinical Findings • Primary (Idiopathic): Unknown etiology, but associated
a stroke that caused ... scapulothoracic) #AdhesiveCapsulitis ... pathophysiology #diagnosis #symptoms ... #signs #stages ... #staging #msk
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