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diagnosis management treatment 21hydroxylasedeficiency 21ohd anatomy cardiomyopathy circulation endocrinology fallot fetal peripartum praderwilli syndrome tetralogy
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... diagnosis #management #cardiology ... #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Signs/Symptoms/Complications ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Peripartum Cardiomyopathy - Summary 1. Definition • Towards the end of pregnancy to 5 months postpartum
exclude other causes ... Genetic predisposition ... early post-partum 9. ... Thromboembolic complications ... diagnosis #management #cardiology
Fetal and Post Transition Circulation In the fetal circulatory system, oxygenated blood is delivered via the umbilical
oxygenated blood passes ... #Circulation #Pathophysiology ... #Cardiology #Anatomy ... #Peds #Pediatrics
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