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diagnosis injury management symptoms differential genetics infant neurology physicalexam predictors traumatic 21hydroxylasedeficiency 21ohd als amyotrophic brudzinskis catch causes cellulitis chalice
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... in an infant Decreased ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... Prader-Willi Syndrome Signs ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
CATCH Predictors for Clinically Significant TBI - GCS Less than 15 at 2 hours post
Predictors for Clinically ... exam - Any Sign ... Predictors #Traumatic #Brain ... Injury #Diagnosis #Peds ... #Pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Differential Diagnosis Algorithm ... Nervous System - Decreased ... Normal Reflexes - Brain ... #Causes #Peds # ... Pediatrics
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 ... #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds
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 Orbital Cellulitis: Pathogenesis and Clinical Findings Definitions: a. Chemosis: Edema of the bulbar conjunctiva b. Panopthalmitis: inflammation of all
Pathogenesis and Clinical ... pupillary defect -> Decreased ... Subperiosteal abscess -> Brain ... Orbital #Cellulitis #pathophysiology ... ophthalmology #diagnosis #signs
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... #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
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... lack of tapering, decreased ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
combination of the clinical ... lateral sclerosis Pathophysiology ... cellular function Clinical ... - Fatigue and decreased ... MRI: Brain, cervical
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