The three-parent baby: Medicolegal, forensic and ethical concerns.
Nandini ChitaraKewal KrishanKanchan TanujPublished in: Medicine, science, and the law (2024)
In the recent past, human genetics and in vitro fertilization (IVF) have undergone various advances to combat with several congenital and developmental disorders. These advances are a boon for the families and patients who were restricted from having a child due to one or the other reasons. One such reason is the mitochondrial DNA (mtDNA) mutations, which are definitely transmitted from the mother to the child due to uniparental/maternal inheritance of mitochondria. Depending upon the range of the mutation (mutation loads) present, the mtDNA mutation leads to various devitalizing to fatal disorders, all of which are incurable. Scientists and researchers developed a technique known as mitochondrial donation technique or mitochondrial replacement therapy (MRT) to combat with the mtDNA mutations. The technique relies on the replacement of faulty mitochondria in the mother's egg with the normal wild-type from a donor female resulting in a "three-parent baby." On the other side, forensic scientists and anthropologists continuously explore the mtDNA in various medicolegal cases and in uncoupling the mystery of human origin and migration respectively. In this regard, we explored the genetic, forensic and ethical aspects of a "three-parent baby." The present communication also attempts to highlight the importance and limitations of the MRT technique/three-parent baby in a medicolegal context.
Keyphrases
- mitochondrial dna
- copy number
- replacement therapy
- endothelial cells
- wild type
- genome wide
- oxidative stress
- mental health
- induced pluripotent stem cells
- cell death
- dna methylation
- smoking cessation
- decision making
- pregnancy outcomes
- physical activity
- pregnant women
- birth weight
- endoplasmic reticulum
- weight gain
- nitric oxide synthase