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physicalexam clinical meningitis sign brudzinskis disease features 21hydroxylasedeficiency 21ohd dehydration diagnosis endocrinology genetics infant kernigs pathophysiology timeline
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Kawasaki Disease ... #Kawasaki #Disease ... #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
Brudzinski's Sign on Physical Exam - Meningitis #Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... #Brudzinskis #Sign ... PhysicalExam #clinical #video ... #neurology #peds ... #pediatrics #meningitis
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 Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features of shock ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
Kernig's Sign in Meningitis Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... In this video, the ... Meningitis #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds #neurology
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 Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
Kawasaki Disease ... Extremities #Kawasaki ... Timeline #Features #Signs ... #Symptoms #Peds ... #Pediatrics
Brudzinski's Sign on Physical Exam - Meningitis via @TheIntern254 #Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics
Brudzinski's Sign ... #Brudzinskis #Sign ... PhysicalExam #clinical #video ... #neurology #peds ... #pediatrics #meningitis
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
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