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21hydroxylasedeficiency cardiology cxr diagnosis falot genetics glftap gravis macroadenoma management masseffects mnemonic myasthenia neurology pituitary radiology tetralogy xray
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
Tetralogy of Falot on Chest X-Ray Tetralogy of Falot comprises four defects - 1. Ventricular septal defect (VSD) 2.
four defects - 1. ... Devpriyo Pal @drdevrad ... #XRay #CXR #clinical ... #radiology #peds ... #pediatrics #cardiology
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
Pathogenesis and Clinical ... approximately 1 ... Signs / Symptoms ... #Macroadenoma #SideEffects ... #endocrinology
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
weakness in: 1. ... EMG Findings: 1. ... test - Cogan sign ... - Peek sign ... Imaging - CT Chest
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