32 results
signs pathophysiology psychiatry criteria physicalexam personalitydisorder neurology behavioraldisorder newborn primitive reflex algorithm babinski differential genetics management pyramidal tone 21hydroxylasedeficiency 21ohd
Scarf Sign (Normal) on Physical Exam The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... The infant's arm ... #clinical #video ... hypotonia #hypotonic #peds ... #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
Kernig's Sign in Meningitis Kernig's sign is present if the patient, in the supine position with the
In this video, the ... infant cries as ... #Meningitis #Clinical ... #Video #PhysicalExam ... #Pediatrics #Peds
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 Positive Babinski Reflex with dorsiflexion of the big toe after stroking the sole of the foot. This
is normal and infants ... flexor response by 12 ... Upgoing #Positive #Peds ... #Pediatrics #Clinical ... #Video #PhysicalExam
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 Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Pathogenesis and Clinical ... Findings Risk ... chromosome 21) Signs ... #diagnosis #signs ... #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
findings • Maternal ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... pathophysiology #peds ... #pediatrics
Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... #Measles #Diagnosis ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings Parasomnias - Micro-arousal episodes during SWS -> Intense activation of
Pathogenesis and clinical ... findings Parasomnias ... #Peds #pathophysiology ... #symptoms #pharmacology ... #diagnosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Findings Autosomal ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... #Findings #Diagnosis ... #Peds #Pediatrics
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