Genetic Risks

Grandparents, parents and children frequently face comparable health issues. You may have inherited risk factors if you have a family history of a specific disease. Inherited risk factors are handed down from parent to kid through DNA. All humans have similar genes, just in different versions.

Deep inside our genetic code lies a complex roadmap of potential health concerns waiting to be uncovered. 

Genetic Risks - Explained.

DNA, also called Deoxyribonucleic Acid, is the essential molecule of life, providing the genetic code for all living species on Earth. DNA is a fascinating molecule essential for trait inheritance and life diversity because genetic instructions are passed down from generation to generation. 

Approximately 99 percent of each person’s genome is similar to every other human. The unique one per cent contains millions of variants, most of which have minimal impact on our health. Scientists have found hundreds of DNA variations that cause or raise a person’s chance of getting the disease.

Many diseases are caused by complicated genetic alterations that interact with lifestyle and environmental variables. However, hundreds of disorders known as Mendelian diseases are a result of alterations in a single gene, which are sufficient to cause the disease on their own.

Genetic risk refers to the possibility or probability that an individual would develop a specific disease or health condition due to their genetic makeup.

 It is determined by the presence or absence of specific genetic variations linked to these disorders. Some genetic variants raise the chance of a disease, while others may give protection. 

Key Genetic Risks to Consider:

Hereditary Cancer Syndromes

Inherited mutations in genes such as BRCA1 and BRCA2 significantly raise the risk of breast and ovarian cancers.

Cardiovascular Diseases

Family history plays a crucial role in the genetic predisposition to heart-related conditions like coronary artery disease and hypertension.

Neurological Disorders

Genetic mutations raise the risk of developing conditions such as Alzheimer’s disease and Parkinson’s disease.

How Are Genetic Risks Identified?

Genetic testing analyses individuals’ DNA to find significant DNA variants and evaluate their susceptibility to specific health conditions. 

A DNA sample is taken for genetic testing, most commonly from blood or saliva. DNA is tested with the help of cutting-edge technology to find genetic code differences. Most genetic testing is focused on genes or gene regions that have been connected to specific disorders.

The test compares an individual’s DNA to a reference sequence and can detect variations that may increase the chance of developing a certain disease. 

Methods for identifying genetic risks:

Genetic Predisposition and Preventive Measures

Having a genetic predisposition to a disease doesn’t mean you will develop the condition. However, it does increase the likelihood. Preventative steps can remarkably lower the risks, allowing individuals to lead healthier lives.

Preventive Strategies:

Genetic Risks

Genetic Risk Factors and Their Impact

While genetic risks cannot be altered, recognising and managing them can minimise their impact on health. Several factors influence genetic risks:

The Role of Genetic Testing in Disease Management

Genetic testing is an integral tool for identifying genetic risks. It offers detailed insights into a genetic makeup and potential health challenges. 

For people with a family history of certain genetic disorders, genetic testing can be a life-changing step toward preventive health management.

Critical Benefits of Genetic Testing:

The Importance of Genetic Counseling

Once genetic risks are identified, genetic counselling plays a vital role in helping people understand and manage them. A genetic counselor explains the implications of genetic test results, provides emotional support, and helps families make informed healthcare decisions.

Why Consider Genetic Counseling?

Consult Dr Lida Anwari to identify your genetic risks

Dr Lida Anwari is a leading genetic risk assessment and counselling expert, helping patients navigate their health journeys with excellent knowledge and confidence. Her advanced training and education make her a trusted expert in handling high-risk pregnancies. She  provides you consultation with her fetal medicine expert knowledge  for optimal prediction and outcomes.

By knowing your genetic predispositions, Dr Anwari can offer personalised care and expert guidance to help you take control of your health.

Are you concerned about your genetic risks? Book an Appointment Today

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