Dr. Jennifer N Silva MD
Cardiologist (Pediatric) | Pediatric Cardiology1 Childrens Pl Suite C Saint Louis MO, 63110
Dr. Silva is a Pediatric Cardiologist. She has a special interest in electrophysiology. Dr. Silva is happy to provide a second opinion on any heart disease diagnosis or heart disease treatment recomme ...
Education and Training
St George',s University
St. George's University School of Medicine
PediatricsAmerican Board of PediatricsABP
- Management of postoperative pediatric cardiac arrhythmias: current state of the art.
- 3:2 antegrade atrioventricular block with AV nodal reentrant tachycardia: what is the mechanism and where is the block?
- Updates on the inherited cardiac ion channelopathies: from cell to clinical.
- Duplication of 20p12.3 associated with familial Wolff-Parkinson-White syndrome.
- Pediatric electrocardiographic imaging applications.
- SPEAR Trial: Smartphone Pediatric ElectrocARdiogram Trial.
- Use of smartphone technology in cardiology.
- The incidence of chromosome abnormalities in neonates with structural heart disease.
- A Clinical Risk Score to Improve the Diagnosis of Tachycardia-Induced Cardiomyopathy in Childhood.
- Heart Disease
- Birth Defects
- Congenital Heart Disease
- Pediatric Cardiology, Washington University Medical School, St Louis, MO 2008
- Pediatric Electrophysiology, Children's Hospital Boston, MA 2009
- Washington University School of Medicine St. Louis Missouri
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Patient Experience with Dr. Silva
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Kawasaki disease is a rare childhood disease that causes inflammation of the arteries in the body. The characteristic symptoms of the disease, which is high fever and peeling skin, remains for almost a week. In most cases, it gets back to normal without any major issues. Children will be monitored...
- What Is Duchenne Muscular Dystrophy? Causes, Symptoms, and Treatment
Muscular dystrophies are a group of diseases that make the muscles of the body weaker over a period of time. The muscles become less flexible in this condition. Out of the nine types of muscular dystrophy, Duchenne muscular dystrophy is one of the most common.The main characteristics of this medical...
- Newborn Diagnosis: Tetralogy of Fallot
Tetralogy of FallotTetralogy of Fallot is a congenital heart defect, which affects the heart’s structure, causing blood with low levels of oxygen to circulate throughout the body. Babies born with tetralogy of Fallot tend to have a blue discoloration of the skin due to low oxygen levels in their...
- What Is Progeria?
Progeria or Hutchinson-Gilford progeria syndrome (HGPS), is a rare genetic condition characterized by a rapidly aging appearance in children. Newborns and infants born with this condition typically look healthy and normal, but may physically display characteristic facial features, such as prominent...
- What Is Neonatal Lupus?
Neonatal lupus is a not so common autoimmune disease. It is not true lupus as all the symptoms will completely disappear after 6 months of age. Neonatal lupus is also known by several other terms. The condition is also called as:...
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