About us

GenePath

About GenePath

GenePath provides evidence and expert-knowledge based guidance, services and support to the public and and clinicians in Bangladesh for the better usage of genetic information to improve health-care outcomes.

We help design genetic tests and explain genetic test results in a clear and personalized way. Our mission is to empower people with the knowledge and tools they need to make informed decisions about their health and well-being.

Our deep knowledge about the genetic basis of human diseases can guide you through the process of genetic testing, from choosing the right test for your needs, to understanding the implications and limitations of the results. We also offer educational resources and support groups for people who are interested in learning more about genetics and its impact on their lives. Whether you are curious about your ancestry, your risk of developing certain diseases, or your family planning options, GenePath can help you find the answers you are looking for.

GenePath may help you understand and decide on the following genetic testings

Newborn screening: This is done just after birth to identify genetic disorders that can be treated early in life. For example, every baby in the UK is tested for cystic fibrosis as part of the heel prick test.

Diagnostic testing: This is done to confirm or rule out a genetic condition if you or your child has symptoms. For example, a blood test can diagnose Fragile X syndrome.

Carrier testing: This is done to find out if you or your partner carry a gene mutation that could cause a genetic disorder in your children. For example, carrier testing can detect mutations for cystic fibrosis, sickle cell disease, or Tay-Sachs disease.

Prenatal testing: This is done during pregnancy to check the health of your baby and detect certain genetic conditions before birth. For example, prenatal testing can detect Down syndrome, spina bifida, or trisomy 18.

Pre-implantation testing: This is done on embryos created through in vitro fertilization (IVF) to select the ones that do not have certain genetic conditions before implanting them in the uterus. For example, pre-implantation testing can prevent passing on Huntington’s disease, cystic fibrosis, or hemophilia.

Predictive testing: This is done to estimate your risk of developing a genetic condition in the future or to guide your medical care. For example, predictive testing can assess your risk of breast cancer, colon cancer, or Alzheimer’s disease.

Forensic testing: This is done to identify individuals using their DNA for legal purposes. For example, forensic testing can be used for paternity testing, crime scene investigation, or identifying human remains.