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neurology 21hydroxylasedeficiency 21ohd amyotrophic anemia aplastic differential encephalopathy endocrinology gravis hematology lateral myasthenia myelitis posterior pres reversible sclerosis syndrome transverse
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 ... • This is also ... Signs/Symptoms/Complications ... #peds #pediatrics
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... lateral sclerosis Pathophysiology ... - Causes progressive ... fasciculations Common Symptoms ... #diagnosis #management
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
Myasthenia Gravis Overview ... Generalized fatigue - ALS ... test - Cogan sign ... - Peek sign ... #management #neurology
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Syndrome (PRES) Overview ... Etiology: • Pathophysiology ... Neurological symptoms ... edema visualized as ... #management #neurology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia - Overview ... Aplastic Anemia Clinical ... and petechiae Causes ... Syndromes: - Genetic ... #management
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
Transverse Myelitis Overview ... • Bilateral signs ... and/or symptoms ... • Infectious causes ... #management #neurology
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