Inherited Cardiovascular Diseases & When Genetic Screening Makes Sense
Genes are responsible for every aspect of the cardiovascular system, from the way heart cells communicate to the strength of blood cells. As such, a genetic mutation (disease-causing variant) in a single gene can increase the likelihood of developing heart disease.
Cardiovascular diseases can be inherited by children from their parents. This is why other family members are encouraged to undergo genetic screening for risk factors when a loved one is diagnosed with heart disease or heart disorder.
Why Would a Genetic Test Be Suggested For My Child?
As a mother or father, you want what's best for your child and their health - it's simply part of being a parent. As such, when they experience health, or developmental concerns arise, it may be suggested that genetic testing be carried out. That said, it’s only in certain circumstances that this would be a suggested course of action.
What is Trisomy 21 & how is it Diagnosed?
Trisomy 21 is the most prevalent chromosomal anomaly in human beings, also referred to as Down Syndrome, Trisomy 21 is a genetic condition that's characterised by an extra chromosome.
Dr Willie Reardon: Expert Medico-Legal Witness Since 1996
Dr Willie Reardon is the founder of Genetics.ie, a company that offers a wide range of genetic testing services, from testing for muscular dystrophies to chromosome disorders. Today, we look at his experience as a medico-legal witness - something he has been doing around the world for over 25 years.
Genetic Testing in Heart Disease
At Genetics.ie we offer a wide range of genetic testing services and today we’re here to talk about its relevance to those with heart disease. Specifically, there are genetic disorders of cardiac function, which may be the underlying reason for the cardiac problem in an individual and their family
Myotonic Dystrophy Explained: A Genetic Condition We Specialise in Diagnosing
As part of a group of inherited disorders known as muscular dystrophies, myotonic dystrophy is the most common form that begins in adulthood. It is characterized by progressive muscle-weakening and wasting and it is a genetic condition, frequently overlooked, that we specialise in diagnosing.
What is Karyotyping & What Is Its Purpose?
The procedure known as Karyotyping is an investigation undertaken by a Clinical Geneticist to examine the chromosomes of an individual patient. The purpose of examining the chromosomes is to determine whether any structural issues or abnormalities exist within them
What is Genetic Counselling?
Basically, genetic counselling refers to providing genetic information, direction as to services and support - something that allows them to make informed decisions about their health - both when the information is positive and negative. However, counselling is always based upon a secure genetic diagnosis.
What To Expect When Using Genetics.ie Services
At Genetics.ie, our goal is to provide prompt, consultant-delivered genetic testing that reflects not only our expertise and experience, but also our commitment to meeting highest clinical standards and most-informed patient care. We offer a wide range of genetic testing, screening and diagnosis services to patients across Ireland from our Blackrock-based clinic.