We can improve the quality of life for children affected by SMA and similar disorders, ensuring they receive the multidisciplinary support and care needed to thrive and lead fulfilled lives.
Understanding the secrets of inherited health conditions not only benefits individuals and families but also advances the frontiers of medical science.
The gene therapy technology from IIT Kanpur will be further developed as an Indigenous Product by Reliance Life Sciences.
There are cases where the couple is not necessarily infertile and yet may benefit from IVF.
The Vice President stressed that focus should be made on preventive measures to address the burden of thalassemia and sickle cell anemia in the country.
Genomics and its adoption in clinical practice has seen a resurgence over the past few years. To enhance read on to know this emerging medical discipline.
Scientists have discovered an inherited condition called TULP3-related ciliopathy, a genetic condition which could help them detect the underlying reasons of kidney or liver failure.
Preimplantation genetic testing (PGT) can be advised to one with recurrent miscarriage, or for a couple who have had children with genetic disorders.
You may be preoccupied with your wedding planning and spending a fortune on your wedding attire, food and decor. Along with that, make sure you are enrolling for some health tests too.
A four-month-old baby has been diagnosed with the rare disease Fibrodysplasia Ossificans Progressiva (FOP) which affects only 1 in 2 million people. Read to know everything about this genetic condition.
Couples having a family history of genetic conditions are likely to pass on the defective genes to their children. But thanks to a new technology, called PGT-M, this can be prevented now.
Today is World Rare Disease Day, which seeks to raise awareness and educate people about conditions that affect maybe 5 people in a population of 10,000.
Diagnosing spinal muscular atrophy
Spinal muscular atrophy is a spinal cord related health condition which mostly affects children.
A study published in the American Journal of Human Genetics has revealed that it could be too early to recommend DNA sequencing for the general public to screen for additional genetic abnormalities and disorders.
We can improve the quality of life for children affected by SMA and similar disorders, ensuring they receive the multidisciplinary support and care needed to thrive and lead fulfilled lives.
Understanding the secrets of inherited health conditions not only benefits individuals and families but also advances the frontiers of medical science.
The gene therapy technology from IIT Kanpur will be further developed as an Indigenous Product by Reliance Life Sciences.
There are cases where the couple is not necessarily infertile and yet may benefit from IVF.
The Vice President stressed that focus should be made on preventive measures to address the burden of thalassemia and sickle cell anemia in the country.
Genomics and its adoption in clinical practice has seen a resurgence over the past few years. To enhance read on to know this emerging medical discipline.
Scientists have discovered an inherited condition called TULP3-related ciliopathy, a genetic condition which could help them detect the underlying reasons of kidney or liver failure.
Preimplantation genetic testing (PGT) can be advised to one with recurrent miscarriage, or for a couple who have had children with genetic disorders.
You may be preoccupied with your wedding planning and spending a fortune on your wedding attire, food and decor. Along with that, make sure you are enrolling for some health tests too.
A four-month-old baby has been diagnosed with the rare disease Fibrodysplasia Ossificans Progressiva (FOP) which affects only 1 in 2 million people. Read to know everything about this genetic condition.
Couples having a family history of genetic conditions are likely to pass on the defective genes to their children. But thanks to a new technology, called PGT-M, this can be prevented now.
Today is World Rare Disease Day, which seeks to raise awareness and educate people about conditions that affect maybe 5 people in a population of 10,000.
Diagnosing spinal muscular atrophy
A study published in the American Journal of Human Genetics has revealed that it could be too early to recommend DNA sequencing for the general public to screen for additional genetic abnormalities and disorders.
Spinal muscular atrophy is a spinal cord related health condition which mostly affects children.
