13 results
diagnosis physicalexam clinical babinski behavioraldisorder genetics management neurology newborn plantar psychiatry pyramidal 21hydroxylasedeficiency 21ohd adhd als alzheimersdisease amyotrophic attentiondeficithyperactivedisorder brudzinskis
Positive Babinski Reflex with dorsiflexion of the big toe after stroking the sole of the foot. This
flexor response by 12 ... Upgoing #Positive #Peds ... #Pediatrics #Clinical ... #Video #PhysicalExam ... #Primitive #pyramidal
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 Plantar Grasp Reflex The plantar grasp reflex is elicited by pressing a thumb against the sole of
Plantar Grasp Reflex ... disappears around 9-12 ... #PhysicalExam #Video ... #Pediatrics #Foot ... #Peds #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 ... myoclonic seizure, primitive ... reflexes, incontinence ... AlzheimersDisease #Dementia #pathophysiology ... #signs #symptoms
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... While the pathophysiology ... an involuntary reflex ... #PhysicalExam #Pediatrics ... #Peds
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 Primitive Suck, Rooting Reflex on Newborn Physical Exam The normal response to stroking the lateral aspect
Primitive Suck, ... toes or “Babinski sign ... Suck #Rooting #Primitive ... PhysicalExam #clinical #video ... #peds #pediatrics
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 Plantar Reflex on Newborn Physical Exam The normal response to stroking the lateral aspect of the
toes or “Babinski sign ... Plantar #Pyramidal #Primitive ... #Babinski #Reflex ... PhysicalExam #clinical #video ... #peds #pediatrics
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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
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
#OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
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 ... endocrinology #peds ... #pediatrics
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
lateral sclerosis Pathophysiology ... of UMN and LMN signs ... of UMN and LMN signs ... both UMN and LMN signs ... EMG: LMN Signs in
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