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21hydroxylasedeficiency diagnosis endocrinology genetics management myasthenia neurology pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... non-arousable, decr urine ... #pathophysiology ... endocrinology #peds
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
Ocular- 50%: Ptosis ... test - Cogan sign ... - Peek sign ... aspiration and acute ... immunosuppressants - Meds
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