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physicalexam dmd gowers muscular neurology sign 21hydroxylasedeficiency 21ohd dehydration endocrinology genetics infant pathophysiology
Gowers' Sign on Physical Exam Seen in this patient with Duchenne muscular dystrophy (DMD) #Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... muscular dystrophy ... PhysicalExam #neurology #clinical ... #video #pediatrics ... #DMD #Duchenne
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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 ... #neurology #clinical ... #video #pediatrics ... #muscular #dystrophy ... #DMD #Duchenne
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 Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
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