15 results
clinical physicalexam reflex normal meningitis sign brudzinskis diagnosis genetics newborn symptoms 21hydroxylasedeficiency 21ohd alzheimersdisease asphyxia asymmetrical atnr babinski dementia escape
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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 The asphyxia escape reflex is assessed by placing the child in the prone position on the
PhysicalExam #clinical #video ... #Neurology #Peds ... #Pediatrics #Normal ... #Primitive
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 Asymmetrical Tonic Neck Reflex (ATNR) This primitive reflex found in newborn babies that normally vanishes around 4
(ATNR) This primitive ... PhysicalExam #clinical #video ... #Neurology #Peds ... #Pediatrics #Normal ... #Primitive
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 Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... / Symptoms / Complications ... myoclonic seizure, primitive ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis
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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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Landau's Reaction (Reflex) on Physical Exam Landau's reaction is investigated holding the baby firmly under the
PhysicalExam #clinical #video ... #Neurology #Peds ... #Pediatrics #Normal ... #Primitive
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 Moro Reflex on Newborn Physical Exam The Moro reflex is obtained by holding the baby’s head and
#Moro #Reflex #Peds ... #Pediatrics #Clinical ... #Video #Neurology ... #PhysicalExam #Primitive
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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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
While the pathophysiology ... Video by Dr. ... Meningitis #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds
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