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neurology dystrophy physicalexam dmd 21hydroxylasedeficiency als amyotrophic diagnosis endocrinology genetics lateral management peds sclerosis
Gowers' Sign on Physical Exam Seen in this patient with Duchenne muscular dystrophy (DMD) #Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... muscular dystrophy ... (DMD) #Gowers ... #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 ... #DMD #Duchenne
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 Gowers' Sign on Physical Exam Caused by proximal muscle weakness typically seen in muscular dystrophy #Gowers #Sign #PhysicalExam
Gowers' Sign on ... Physical Exam Caused ... #Sign #PhysicalExam ... #neurology #clinical ... #video #pediatrics
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 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 ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
lateral sclerosis Pathophysiology ... - Causes progressive ... 4) progressive muscular ... Upper extremity, lower ... fasciculations Common Symptoms
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