6 results
diagnosis syndrome 21hydroxylasedeficiency barre differential encephalopathy gbs genetics gravis guillain myasthenia myelitis pediatrics posterior pres renal reversible rheumatology scleroderma src
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
test - Cogan sign ... - Peek sign ... Myasthenia Crises ... Gravis #diagnosis #management ... #neurology
Guillain-Barré Syndrome (GBS) Acute autoimmune demyelinating polyradiculoneuropathy that presents with rapidly progressive flaccid weakness Epidemiology: • Incidence: 1
infection that cross-reacts ... , Epstein-Barr virus ... the underlying pathophysiology ... Syndrome #diagnosis #management ... #neurology
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
• Hypertensive crisis ... may precede the neurologic ... Etiology: • Pathophysiology ... Syndrome #diagnosis #management ... #neurology
Scleroderma Renal Crisis (SRC) Clinical Presentation of Scleroderma Renal Crisis: 1) Acute kidney injury 2) Abrupt onset of hypertension 3)
anemia (MAHA) Pathophysiology ... of arteries Management ... , add other BP meds ... #rheumatology #nephrology ... #diagnosis #management
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
monophasic Pathophysiology ... • Bilateral signs ... than 2/3 of the cross-sectional ... Myelitis #diagnosis #management ... #neurology #differential
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