VEXAS Syndrome: Half Of Patients, Mostly Men, Die Within 5 Years Of Diagnosis
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.
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.
Interpreting the results of genetic testing can be complex; genetic counsellors can help you understand the exact impact of the disease on your body.
From preconception screening to testing hereditary disease, let us have a look at various ways Genetic Testing has been helping millions of people today.
How To Tackle Childhood Cancers With The Power Of Genetic Testing?
World Cancer Day 2023 marks the second year of the campaign "close the care gap." Should you take genetic tests for cancer?
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.
Regular health check-up, including tests such as an echocardiogram, is suggested for anyone above 35 years.
How To Overcome Genetic Predispositions For A Longer Life? Explains Fitness Expert Meenakshi Mohanty
Genomics has helped better understand and managed liver and gastrointestinal (GI) diseases, including those which are labelled as "idiopathic" disorders.
Father donates a portion of his liver to save his 23-day-old baby from a rare hereditary disorder. Read on to know more about Galactosemia.
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.
There are cases where the couple is not necessarily infertile and yet may benefit from IVF.
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.
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.
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.
Down Syndrome is a genetic condition that has no cure as yet. But it can be managed very well with love and care. Read on to know it all.
Von Hippel-Lindau syndrome is a rare hereditary condition characterized by the formation of tumours and cysts in multiple organs, including the brain.
Experts at Jaslok Hospital did a study that revealed a first-in-the-world medical report that showed life-threatening side effects with some antivirals in individuals with a genetic abnormality.
From preconception screening to testing hereditary disease, let us have a look at various ways Genetic Testing has been helping millions of people today.
How To Tackle Childhood Cancers With The Power Of Genetic Testing?
World Cancer Day 2023 marks the second year of the campaign "close the care gap." Should you take genetic tests for cancer?
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.
Regular health check-up, including tests such as an echocardiogram, is suggested for anyone above 35 years.
How To Overcome Genetic Predispositions For A Longer Life? Explains Fitness Expert Meenakshi Mohanty
Genomics has helped better understand and managed liver and gastrointestinal (GI) diseases, including those which are labelled as "idiopathic" disorders.
Father donates a portion of his liver to save his 23-day-old baby from a rare hereditary disorder. Read on to know more about Galactosemia.
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.
There are cases where the couple is not necessarily infertile and yet may benefit from IVF.
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.
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.
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.
Down Syndrome is a genetic condition that has no cure as yet. But it can be managed very well with love and care. Read on to know it all.
Von Hippel-Lindau syndrome is a rare hereditary condition characterized by the formation of tumours and cysts in multiple organs, including the brain.
Experts at Jaslok Hospital did a study that revealed a first-in-the-world medical report that showed life-threatening side effects with some antivirals in individuals with a genetic abnormality.
Cardiovascular diseases are increasing among men and women but scientists have found a way to detect the condition early on. They believe it can help reduce the risk of the disease.
Most of the cancers, if detected timely can be cured with better management. It is important to undergo regular health check-up to understand our current health status and for early detection of any abnormalities.
If you are not careful, then hearing loss or deafness can affect anyone as there are many factors that lead to the problem. Here is everything you need to know about it.