17 results
peds signs treatment cardiology disease hematology hemophagocytic hlh lymphohistiocytosis neurology newborn 21hydroxylasedeficiency 21ohd anomalous antenatal aphasia atrioventricular brocas bronchiolitis chagas
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Ventricular septal defect ... #Fallot #Peds #Pediatrics ... #Cardiology #Signs ... #Symptoms #Diagnosis
Atrioventricular Septal Defect aka AV canal defect aka endocardial cushion defect • Epidemiology and Associations • Embryology
Physical Exam • Pathophysiology ... Post-Operative ICU Management ... endocardial #cushion #diagnosis ... #management #peds ... #pediatrics #cardiology
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
diabetes algorithm #Infant ... Diabetic #Mother #Pediatrics ... #NICU #OBGYN #Diagnosis ... #Pathophysiology ... #PatientInfo #Management
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Affects children ... Early diagnosis ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... PVO Present • Diagnosis ... Classic “snowman sign ... Return #TAPVR #diagnosis ... #peds #pediatrics
Bronchiolitis Bronchiolitis is a viral inflamation of the bronchioles and the commonest LRTI in under 1s'. It's
Diagnosis - Coryzal ... symptoms for 1 ... REMEMBER - infants ... Bronchiolitis #pediatrics ... #diagnosis #management
Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
Aphasia - Pathophysiology ... Contralateral sensory deficits ... #Aphasia #Pathophysiology ... #diagnosis #signs ... #symptoms #Brocas
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
#OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
Croup Diagnosis and Management Pearls Common childhood illness, usually viral and self limiting. Characterised by a seal-like
Croup Diagnosis ... and Management Pearls ... Commonly affects ... PeterboroughEM #Croup #Diagnosis ... #Management #pediatrics
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