This is an archive article published on March 1, 2021
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Worried about risk of genetic disorders among kids? This is how IVF can help

Genetic disorder is any disease triggered by a change in the DNA sequence either in fragments or whole.

genetic disorders among kids, what are genetic disorders, what causes genetic disorders, genetic disorders and IVF, health, parenting, indian express newsBabies who suffer from genetic disorders can be at high risk of mental and physical problems, physical abnormalities, and lifelong illnesses. (Photo: Pixabay)
5 min readNew DelhiMar 1, 2021 06:26 PM IST First published on: Mar 1, 2021 at 06:26 PM IST

By Dr Rohit Gutgutia

Parents always take umpteen number of precautionary measures to ensure that their babies are safe and healthy. While the present generation of parents are often going above and beyond to educate themselves about various medical frontiers to secure the future of their child, there are still a few grey areas where creating awareness is essential. One of such is the importance of genetic testing and its role in treating childhood onset disorders.

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Genetic disorder is any disease triggered by a change in the DNA sequence either in fragments or whole. Some people carry genes of genetic illnesses in dormant form and might not show any symptoms themselves, as symptoms are caused only if two of the problem genes are inherited. In case of babies with genetic disorders, some are hereditary, which means that it is passed on from their parents. Other genetic changes can totally be alien to the baby. These chromosome abnormalities produce more than 50 percent of first trimester miscarriages and are found in a third of the foetuses with major malformations. Couples of reproductive ages have a 3 percent chance of having an abnormal child. Babies who suffer from genetic disorders can be at high risk of mental and physical problems, physical abnormalities, and lifelong illnesses. Some of the common genetic disorders among children are thalassemia, sickle cell disease, cystic fibrosis, spinal muscular atrophy, fragile X and hemophilia.

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