9 results
video breathing respiratory duchenne genetics gowers muscular neurology paradoxical pathophysiology 21hydroxylasedeficiency 21ohd brudzinskis dehydration descent endocrinology hoovers infant meningitis praderwilli
Gowers' Sign on Physical Exam Seen in this patient with Duchenne muscular dystrophy (DMD) #Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... (DMD) #Gowers ... #Sign #PhysicalExam ... #neurology #clinical ... #video #pediatrics
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 Tracheal Descent Sign Paradoxical inward movement of the trachea during inspiration. Seen in this COPD patient in
Tracheal Descent Sign ... Tracheal #Descent #Sign ... #clinical #video ... #physicalexam # ... respiratory #pulmonary
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 Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... Pale or Mottled Skin ... #Signs #Symptoms ... #Dehydration #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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 Paradoxical Breathing on Physical Exam Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... Paradoxical #Breathing #PhysicalExam ... #respiratory #clinical ... #video #pulmonary ... #peds #pediatrics
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 Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Brudzinski's sign ... #Meningitis #Clinical ... #Video #PhysicalExam ... #Pediatrics #Peds
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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Loss of parental copy ... Prader-Willi Syndrome Signs ... pathophysiology #peds ... #pediatrics
Hoover's sign on Physical Exam Paradoxical inward movement of the rib cage with inspiration seen in patients
Hoover's sign on ... patients with COPD ... #Hoovers #sign ... #PhysicalExam # ... Clinical #Video
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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 ... Signs/Symptoms/Complications ... & mottled skin. ... endocrinology #peds ... #pediatrics
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