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diagnosis disease pathophysiology genetics physicalexam timeline 21hydroxylasedeficiency 21ohd alzheimersdisease cirrhosis clinical congenital dehydration elbow endocrinology evaluation fallot findings heartdisease hepatology
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
Practical Pediatric Viral Rash Algorithm Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... Viral Rash Algorithm ... five days and no signs ... / symptoms of sepsis ... #Pediatrics #Peds
Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
Kawasaki Disease ... of the 5 other features ... Extremities #Kawasaki ... #Signs #Symptoms ... #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
Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... AlzheimersDisease #Dementia ... pathophysiology #geriatrics ... #diagnosis #signs ... #symptoms
Algorithm for the Evaluation and Management of Suspected Congenital Heart Disease in Neonates Neonates with undiagnosed congenital
Algorithm for the ... with nonspecific symptoms ... #HeartDisease #Algorithm ... Neonates #Neonatal #Peds ... #Pediatrics #Cardiology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Incr Skeletal fractures ... pathophysiology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
suspected incomplete Kawasaki ... other suggestive features ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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