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duchenne dystrophy gowers neurology pathophysiology physicalexam 21hydroxylasedeficiency 21ohd diagnosis disease endocrinology features kawasaki kopliks measles praderwilli syndrome
Gowers' Sign on Physical Exam Seen in this patient with Duchenne muscular dystrophy (DMD) #Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... dystrophy (DMD) ... #Gowers #Sign ... PhysicalExam #neurology #clinical ... #video #pediatrics
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 Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... PraderWilli #Syndrome #genetics ... pathophysiology #peds ... #pediatrics
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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 Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
Kawasaki Disease - Timeline ... of Clinical Features ... #Features #Signs ... #Symptoms #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 ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
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