#HumFitTohIndiaHit: Know how Preimplantation Genetic Testing (PGT) improves IVF success rates by screening embryos for genetic conditions, reducing risks and increasing chances of a healthy pregnancy.
Non-invasive prenatal testing (NIPT) is a simple blood test during pregnancy that helps detect rare genetic conditions early, enabling timely medical guidance and informed decision-making.
This breakthrough in gene editing therapy offers hope not just for hereditary angioedema patients but also for the broader landscape of genetic disorders.
The Pre and Post-test Genetic counselling can be provided at premarital, antenatal, and postnatal stages.
Polycystic Liver Disease (PLD) can cause enlargement of liver and even liver failure. But this genetic disorder is usually asymptomatic.
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.
Most children with Crouzon's Syndrome can have a normal life expectancy if diagnosed early and treated timely.
The child was first treated with chemotherapy, followed by the stem cell transplant. Get to know more about Familial HLH and its signs and symptoms.
Spinal Muscular Atrophy is genetic disorder seen in one in 10,000 live-born babies, but is the most common cause of death in the infantile age group.
Consanguineous marriages are associated with the occurrence of hereditary and multifactorial diseases. Read on to know all about it.
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.
Be part of the International Thalassaemia Day 2022 and help transform the lives of millions of people suffering from this disease.
"Identifying the causal variant(s) in a patient with a rare disorder is like pointing out a needle in a haystack"
Preimplantation genetic testing (PGT) can be advised to one with recurrent miscarriage, or for a couple who have had children with genetic disorders.
Whether or not having a consanguineous relationship increases the incidence of genetic disorders in the offspring has been a part of heated debate for years. Here is how it might affect pregnancy.
The boy who was born with the rare genetic disorder gradually lost his ability to walk and stand and was depending on a wheelchair for mobility.
#HumFitTohIndiaHit: Know how Preimplantation Genetic Testing (PGT) improves IVF success rates by screening embryos for genetic conditions, reducing risks and increasing chances of a healthy pregnancy.
Non-invasive prenatal testing (NIPT) is a simple blood test during pregnancy that helps detect rare genetic conditions early, enabling timely medical guidance and informed decision-making.
This breakthrough in gene editing therapy offers hope not just for hereditary angioedema patients but also for the broader landscape of genetic disorders.
The Pre and Post-test Genetic counselling can be provided at premarital, antenatal, and postnatal stages.
Polycystic Liver Disease (PLD) can cause enlargement of liver and even liver failure. But this genetic disorder is usually asymptomatic.
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.
Most children with Crouzon's Syndrome can have a normal life expectancy if diagnosed early and treated timely.
The child was first treated with chemotherapy, followed by the stem cell transplant. Get to know more about Familial HLH and its signs and symptoms.
Spinal Muscular Atrophy is genetic disorder seen in one in 10,000 live-born babies, but is the most common cause of death in the infantile age group.
Consanguineous marriages are associated with the occurrence of hereditary and multifactorial diseases. Read on to know all about it.
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.
Be part of the International Thalassaemia Day 2022 and help transform the lives of millions of people suffering from this disease.
"Identifying the causal variant(s) in a patient with a rare disorder is like pointing out a needle in a haystack"
Preimplantation genetic testing (PGT) can be advised to one with recurrent miscarriage, or for a couple who have had children with genetic disorders.
Whether or not having a consanguineous relationship increases the incidence of genetic disorders in the offspring has been a part of heated debate for years. Here is how it might affect pregnancy.
The boy who was born with the rare genetic disorder gradually lost his ability to walk and stand and was depending on a wheelchair for mobility.
This rare genetic disorder is widely misunderstood in India.
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