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signs features pathophysiology physicalexam timeline 21hydroxylasedeficiency 21ohd algorithm aliem bruising cardiology cirrhosis criteria dehydration endocrinology facial fallot findings genetics hepatology
Kawasaki Disease - Clinical Criteria #Diagnosis #Peds #Pediatrics #Kawasaki #Disease #Manifestations #Criteria #ALiEM
Kawasaki Disease ... - Clinical Criteria ... #Diagnosis #Peds ... #Pediatrics #Kawasaki ... #Disease #Manifestations
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Kawasaki Disease ... #Kawasaki #Disease ... #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
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
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms ... #Diagnosis
Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
Kawasaki Disease ... - Timeline of Clinical ... #Features #Signs ... #Symptoms #Peds ... #Pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Disease 1. ... Infants ≤6 months ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... of Liver Disease ... #LiverFailure #Signs ... #Findings #Diagnosis ... #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 ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... pathophysiology #diagnosis ... #symptoms #signs ... #peds #pediatrics
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