Pediatric Cardiology and Genetics

The study of Pediatric Cardiology is responsible for the diagnosis of congenital heart defects, performing diagnostic procedures such as echocardiograms, cardiac catheterizations and electrophysiology studies. The increasing number of neonates with congenital heart defects referred to the neonatal intensive care unit reflects the increasing awareness that the defects may be present. Chest radiography and ECG rarely assist in the neonatal diagnosis. Congestive heart failure in the fetus, or hydrops, can be detected by performing fetal echocardiography. In this case, congestive heart failure may represent underlying anemia (e.g. Rh sensitization, fetal-maternal transfusion), arrhythmias (usually supraventricular tachycardia), or myocardial dysfunction (myocarditis or cardiomyopathy). Many of the Pediatric heart defects such as patent ductus arteriosus interruption, vascular ring division, pericardial window, diaphragm placation, thoracic duct ligation, ligation of collateral vessels have been repaired using Pediatric interventional cardiology. The barriers and challenges to achieving routinely applicable Tissue Engineered and Regenerative Cardiac Surgery Methods are also explored as is a novel concept for the Cardiac Hybrid Operating Room Suite of the 21st Century. Apart from these techniques nursing and care for Pediatric cardiac patients also plays an important role for the cure of Pediatric cardiac patients.

Most children are born healthy with no medical problems or birth defects. However, some children are born with differences in body structure, brain development, or body chemistry that can lead to problems with health, development, school performance, and/or social interaction. Pediatric geneticists are trained to identify the causes and natural history of these disorders. They may suggest tests and treatments that can help in understanding and caring for your child’s condition. Pediatric geneticists also can help families understand whether some conditions are hereditary (coming from the genes) and offer testing to family members who may be at risk for having children with similar problems.

Related Conferences: Pediatrics Conferences September 14-16, 2016 Amsterdam, The Netherlands; Pediatric Surgery Conferences September 14-16, 2016 Amsterdam, Netherlands; Pediatric Dermatology Conferences October 10-11, 2016 Manchester, UK; Neonatology Conferences November 14-16, 2016 Valencia, Spain; Neonatal Conferences November 14-16, 2016 Valencia, Spain; Pediatric Neurology Conference November 14-16, 2016 Valencia, Spain;  14th International Child Neurology Congress May 1-5 2016, The Netherlands; Child Neurology Society 45th Annual Meeting October 26-29 2016, Canada; British Paediatric Neurology Association Annual Conference January 27-29 2016, UK; 3rd Pan-Slavic Congress of Child Neurology October 19-22 2016, Croatia; International Conference Of Pediatric Neurology of Egyptian Specialized Society of pediatric Neurology And Neurodisability March 2-3 2016, Egypt

  • Congestive heart failure
  • Acyanotic congenital heart disease
  • Cyanotic congenital heart disease
  • Rheumatic fever
  • Carditis
  • Arrhythmias
  • Vascular rings and slings
  • Prenatal genetic screening and testing
  • Congenital malformation and teratogenesis
  • Common chromosomal disorders
  • Inborn errors of metabolism
  • Inherited connective tissue disorders
  • Genetic testing and gene therapy
  • Basic genetics principles

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