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diagnosis neurology management 21hydroxylasedeficiency 21ohd comatose encephalopathy genetics gravis myasthenia myelitis pediatrics physicalexam posterior pres reversible syndrome transverse
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... 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
muscles: “myasthenic crises ... life-threatening Differential ... - Peek sign ... 2. ... Myasthenia Crises
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
• Hypertensive crisis ... Etiology: • Pathophysiology ... Reversible course Differential ... the underlying cause ... until cause identified
The Neurological Evaluation of a Comatose Patient Definition: • Coma: a state of unresponsiveness; the absence of
consciousness Differential ... • Mutism Pathophysiology ... safe to stop 2. ... • Examine for signs ... Casey Albin MD @
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
monophasic Pathophysiology ... develops later 2. ... • Bilateral signs ... - More than 2/ ... management #neurology #differential
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