Recent technological advancements have empowered scientists to detect DNA changes with unprecedented precision.
In a shocking and concerning trend, heart-related diseases have claimed the lives of an increasing number of young individuals in 2023. Dr. Abhijit Borse delves deep into the issues.
As research continues to expand our understanding of childhood epilepsy, these specialized professionals will provide neurological care.
Learn these facts about your genes.
The contrast between genetic influences and environmental shifts underscores the dynamic interplay between evolution, genetics, and changing lifestyles in human populations.
LAD is a "primary immunodeficiency" that causes patients to be "abnormally susceptible to developing frequent soft-tissue infections, gum inflammation, and tooth loss". The rare genetic disease basically prevents the body's immune system from functioning normally.
Following certain lifestyle choices can help in reducing diabetes risk.
Every woman should prioritize her health and advocate for herself by staying informed, attending regular medical checkups, and promptly reporting any unusual symptoms to medical personnel.
Understanding cancer's hereditary and genetic aspects is crucial for effective prevention, early detection, and targeted treatment.
Chondrodysplasia is a rare genetic disorder that affects the skeletal system of those who inherit it.
Tailored dietary advice emphasizing antioxidant-rich foods can help mitigate oxidative stress and its associated effects on overall health during menopause.
Restless leg syndrome may be genetic in some cases but in others it may be triggered by certain lifestyle habits as well.
Understanding the secrets of inherited health conditions not only benefits individuals and families but also advances the frontiers of medical science.
The Pre and Post-test Genetic counselling can be provided at premarital, antenatal, and postnatal stages.
There is a higher chance that couples will share a larger percentage of genes when a sizable segment of the population engages in consanguineous marriage.
Diligent adherence to lifestyle modifications empowers individuals with diabetes to achieve significant improvements and remission.
5 genetic variables may also result in non-alcoholic liver disease (NAFLD).
PGT is a primary diagnostic tool to prevent any known genetic disorder transmission.
Polycystic Liver Disease (PLD) can cause enlargement of liver and even liver failure. But this genetic disorder is usually asymptomatic.
Assessing other family members for ASD typically involves a combination of genetic counselling, medical evaluation, and behavioural screening.
On Mother's Day, Dr Mokshadayini of MedGenome Labs highlights the importance of Non-Invasive Prenatal Testing (NIPT) testing for expectant mothers.
Mitochondrial Replacement Therapy (MRT) may be a viable option for couples who are struggling with fertility challenges due to mitochondrial disease, says Dr Kshitiz Murdia.
Osteogenesis imperfecta (OI) is a rare genetic disorder, affecting 1 in 10,000 individuals. Parita Dholakia, an OI warrior, shares some of major challenges faced by OI patients like her.
The chances of having a baby with Down Syndrome increases with increasing maternal age. What can be done to reduce the risk of down syndrome in babies? Dr Anurag Gupta answers the question here.
In a shocking and concerning trend, heart-related diseases have claimed the lives of an increasing number of young individuals in 2023. Dr. Abhijit Borse delves deep into the issues.
As research continues to expand our understanding of childhood epilepsy, these specialized professionals will provide neurological care.
The contrast between genetic influences and environmental shifts underscores the dynamic interplay between evolution, genetics, and changing lifestyles in human populations.
LAD is a "primary immunodeficiency" that causes patients to be "abnormally susceptible to developing frequent soft-tissue infections, gum inflammation, and tooth loss". The rare genetic disease basically prevents the body's immune system from functioning normally.
Following certain lifestyle choices can help in reducing diabetes risk.
Every woman should prioritize her health and advocate for herself by staying informed, attending regular medical checkups, and promptly reporting any unusual symptoms to medical personnel.
Understanding cancer's hereditary and genetic aspects is crucial for effective prevention, early detection, and targeted treatment.
Chondrodysplasia is a rare genetic disorder that affects the skeletal system of those who inherit it.
Tailored dietary advice emphasizing antioxidant-rich foods can help mitigate oxidative stress and its associated effects on overall health during menopause.
Restless leg syndrome may be genetic in some cases but in others it may be triggered by certain lifestyle habits as well.
Understanding the secrets of inherited health conditions not only benefits individuals and families but also advances the frontiers of medical science.
The Pre and Post-test Genetic counselling can be provided at premarital, antenatal, and postnatal stages.
There is a higher chance that couples will share a larger percentage of genes when a sizable segment of the population engages in consanguineous marriage.
Diligent adherence to lifestyle modifications empowers individuals with diabetes to achieve significant improvements and remission.
5 genetic variables may also result in non-alcoholic liver disease (NAFLD).
PGT is a primary diagnostic tool to prevent any known genetic disorder transmission.
Polycystic Liver Disease (PLD) can cause enlargement of liver and even liver failure. But this genetic disorder is usually asymptomatic.
Assessing other family members for ASD typically involves a combination of genetic counselling, medical evaluation, and behavioural screening.
On Mother's Day, Dr Mokshadayini of MedGenome Labs highlights the importance of Non-Invasive Prenatal Testing (NIPT) testing for expectant mothers.
Mitochondrial Replacement Therapy (MRT) may be a viable option for couples who are struggling with fertility challenges due to mitochondrial disease, says Dr Kshitiz Murdia.
Osteogenesis imperfecta (OI) is a rare genetic disorder, affecting 1 in 10,000 individuals. Parita Dholakia, an OI warrior, shares some of major challenges faced by OI patients like her.
The chances of having a baby with Down Syndrome increases with increasing maternal age. What can be done to reduce the risk of down syndrome in babies? Dr Anurag Gupta answers the question here.
VEXAS Syndrome occurs rarely but carries a high mortality rate. It mostly affects men over 50. Read on to know more about this autoimmune condition.
The gene therapy technology from IIT Kanpur will be further developed as an Indigenous Product by Reliance Life Sciences.
