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diagnosis neurology clinical dmd dystrophy muscular physicalexam syndrome video als amyotrophic causes distal encephalopathy gitelman hypokalemia lateral pathophysiology posterior pres
Gowers' Sign on Physical Exam Seen in this patient with Duchenne muscular dystrophy (DMD) #Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... this patient with Duchenne ... #Sign #PhysicalExam ... #neurology #clinical ... #video #pediatrics
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 Gowers' Sign on Physical Exam Indicative of proximal muscle weakness in muscular dystrophy. #Gowers #Sign #PhysicalExam #neurology #clinical
Gowers' Sign on ... #Gowers #Sign #PhysicalExam ... #neurology #clinical ... #video #pediatrics ... dystrophy #DMD #Duchenne
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 Distal Renal Tubular Acidosis (RTA) Type 1 Totally scuppers the kidney's acidification mechanism. Will be
Renal Tubular Acidosis ... secretion Cannot lower ... Distal #Diagnosis #Management ... #Nephrology #Causes ... #Differential #
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of UMN and LMN signs ... Upper extremity, lower ... conditions listed in differential ... Lateral #Sclerosis #neurology ... #diagnosis #management
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Blood transfusion, Hypercalcemia ... Reversible course Differential ... BP lowering - Lower ... Syndrome #diagnosis #management ... #neurology
Gitelman Syndrome Overview What? • Inherited (AR) hypokalemic salt-losing tubulopathies affecting the thiazide-sensitive sodium chloride cotransporter • Gitelman's syndrome
ratio 0.5%) Differential ... Renal tubular acidosis ... Syndrome #diagnosis #nephrology ... #management #pathophysiology ... #Hypokalemia
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