Pediatric Cancer Genomics

Pediatric cancer is generating genetically. The roots of pediatric cancer are hidden deep within the infant’s or child’s DNA. Cancer begins when changes in DNA trigger cells to grow out of control. Genetic predisposition for infant cancer is under diagnosis. Types of genetic testing are Karyotype test, Fluorescence In Situ Hybridization test (FISH), DNA sequencing test, Deletion/Duplication test, Methylation analysis test, SNP chromosome microarray test, and Uniparental disomy test.

 

  • Congenital heart disease in newborns
  • Spina Bifida
  • Parental Obesity
  • Cleft lip and cleft palate
  • Congenital dislocated hip
  • Congenital malformations of genital organs
  • Deformations of the musculoskeletal system
  • Down syndrome
  • Club foot
  • Phenylketonuria

Related Conference of Pediatric Cancer Genomics

Pediatric Cancer Genomics Conference Speakers