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21hydroxylasedeficiency diagnosis genetics gravis myasthenia neurology
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 ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
weakness in: 1. ... EMG Findings: 1. ... - Peek sign ... Imaging - CT Chest ... Gravis #diagnosis #management
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