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diagnosis management 21hydroxylasedeficiency 21ohd congenital diagram fallot fontan neurology posterior praderwilli pres procedure reversible schematic tetralogy treatment
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... Syndromes • “Pink ... diagnosis #management #cardiology ... #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... #PraderWilli #Syndrome ... #genetics #pathophysiology ... #peds #pediatrics
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Posterior Reversible Encephalopathy ... • Headache • Seizures ... Etiology: • Pathophysiology ... : Treat with AEDs ... Posterior #Reversible #Encephalopathy
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Fontan Procedure Schematic A Fontan is done in most children (approximately 90%) who effectively have a single
or a congenital syndrome ... Diagram #congenital #Cardiology ... #Peds #Pediatrics ... #Pathophysiology
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