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diagnosis pediatrics management symptoms signs genetics hsp nejm radiology rheumatology sign syndrome vasculitis 21hydroxylasedeficiency 21ohd alkaptonuria ammonia aortic aorticvalve aortoenteric
Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Introduction & Pathophysiology ... Epidemiology • Clinical ... AorticValve #cardiology #peds
Schematic representation of the major sources of ammonia production and its excretory pathway (GI = gastrointestinal,
pathway (GI = gastrointestinal ... Reye syndrome (Peds ... deficiency #Ammonia #Pathophysiology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Metformin Associated Lactic Acidosis (MALA) Pathophysiology of MALA - Metformin interferes with the activity of the
Acidosis (MALA) Pathophysiology ... Abdominal pain, gastrointestinal ... presentation - Clinical
Diagnosis of IgA Vasculitis (Henoch-Schönlein Purpura) - French Vasculitis Study Group 1) Suggestive clinical manifestations
1) Suggestive clinical ... individuals - Clinical ... patients - Gastrointestinal ... #Rheumatology #Peds
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
Pathogenesis and Clinical ... vasculitis (100%) - Gastrointestinal ... HenochScholeinPurpura #Pathophysiology
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
While the pathophysiology ... Sign #Meningitis #Clinical ... PhysicalExam #Pediatrics #Peds
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 Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... #OtitisMedia #pathophysiology ... symptoms #signs #peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Bronchiolitis - Pathophysiology and Clinical Features #Pediatrics #Peds #Pathophysiology #Bronchiolitis
Bronchiolitis - Pathophysiology ... and Clinical Features ... #Pediatrics #Peds ... #Pathophysiology
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