late pathophysiology lights symptoms signs cardiology endocrinology primary vasculitis 21ohd

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

Signs/Symptoms/Complications ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology

Adhesive Capsulitis (Frozen Shoulder) - Pathogenesis and Clinical Findings

• Primary (Idiopathic): Unknown etiology, but associated

Findings • Primary ... Severe, worse at night ... FrozenShoulder #pathophysiology ... #diagnosis #symptoms ... #signs #stages

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