Follow Whatsapp Channel
Saturday, Jul 19, 2025
In a tribal colony with 120 families, he is one of the first to be diagnosed with sickle cell anaemia, a genetic disorder inherited from parents.
No issues were detected in the child's condition in the seven scannings.
The results would be ready within two weeks. If genetic mutations are detected, then expert medical practitioners and counsellors would suggest suitable options including treatment.
Sickle-shaped cells in an affected person are prone to clotting and cause a range of symptoms, including chronic pain, organ damage, and increased susceptibility to infections.
Bone marrow transplant is a curative option for thalassemia major patients, and it can replace defective bone marrow with healthy bone marrow stem cells from a compatible donor.
A baby's genes can vary greatly from birth, but certain factors inherited from the mother can protect babies from a variety of infections for up to six or seven months.
Rubin’s mother is ready to donate one of her kidneys too to her dear son after two months.
When you are doing a genetic test on a newborn baby, you should remember that you are not doing a diagnosis for all genetic diseases.
Down syndrome can lead to some health complications, and they are at risk for congenital heart disease, respiratory disease, and an increased chance of leukaemia.
Toddler Nirvaan was diagnosed with Spinal Muscular Atrophy (SMA), a rare genetic disorder. Doctors informed his parents that the treatment would cost about Rs 17.5 crore, as they have to procure a costly one-time drug.
Results 1-10 of 18
You can always sign back in at any time.
You have reached the maximum number of saved items. Please remove some items.
