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physicalexam neurology newborn genetics pathophysiology primitive reflex tone 21hydroxylasedeficiency 21ohd babinski dehydration diagnosis endocrinology examination hand hypotonia hypotonic kernigs normal
Brudzinski's Sign on Physical Exam - Meningitis #Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... #Sign #PhysicalExam ... #clinical #video ... #neurology #peds ... #pediatrics #meningitis
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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 ... #Sign #Meningitis ... #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds
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 Brudzinski's Sign on Physical Exam - Meningitis via @TheIntern254 #Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics
Brudzinski's Sign ... #Sign #PhysicalExam ... #clinical #video ... #neurology #peds ... #pediatrics #meningitis
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 Brudzinski's sign is a physically demonstrable symptom of meningitis. It is characterized by reflexive flexion of
Brudzinski's sign ... physically demonstrable symptom ... of meningitis. ... #Brudzinskis #sign ... #clinical #video
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 Kernig's Sign in Meningitis Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... sign is present ... Prakash #Kernigs #Sign ... #Meningitis #Clinical ... #Pediatrics #Peds
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 Scarf Sign (Normal) on Physical Exam The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... Exam The scarf sign ... #Scarf #Sign #PhysicalExam ... #clinical #video ... #pediatrics #tone
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 Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... dehydration in an infant ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Peds #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Pathogenesis and clinical ... Signs/Symptoms ... pathophysiology #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 ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... of meningitis. ... are observed for signs ... #Examination #Peds ... #Pediatrics #Diagnosis
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