Sudden Adult Death Syndrome (SADS) & The Relevance of Genetic Testing in This Situation
At Genetics.ie, we offer a wide array of genetic testing services under the supervision of Dr Willie Reardon, someone with much experience in his field. Today, we're here to talk about a condition known as Sudden Adult Death Syndrome and how genetic testing can help.
What is Collagenopathy?
Collagenopathy is a term that covers a group of rare disorders that affect the body’s connective tissue. Connective tissue supports the body’s organs and joints, providing a framework for the mechanics of internal organ position and function and collagenopathies refer to disorders of collagen which may manifest clinically in disorders such as excess joint laxity, weakness of the arteries, propensity to haemorrhage, scoliosis and a host of other clinical signs.
Muscular Dystrophy - What is it & How is it Diagnosed?
The term muscular dystrophies (MD) describes a group of genetic conditions which cause the muscles to gradually weaken, resulting in increasing disability. MD is a progressive condition, meaning that it worsens over time, often affecting a particular muscle group before eventually affecting others on a more widespread basis.
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.
Who is Dr Willie Reardon - the Founder of Genetics.ie?
All genetics testing services offered by Genetics.ie are carried out under the supervision of Dr Willie Reardon. As you can see, his experience and expertise spans many decades at some of the world’s most prestigious medical institutions. As such, as a patient with us, you’re in very good hands, irrespective of the service required.
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 The Purpose of Carrier Testing & Who Is It For?
Essentially, carrier testing (a.k.a. carrier screening) is a form of genetic test that determines whether an individual carries a gene for a specific genetic disorder. Usually conducted either before or during pregnancy, it’s an important step taken to identify a couple’s chances of having a child with the same genetic disorder.
What Is Clinical Genetics?
What is clinical genetics? Well, essentially, clinical geneticists are Doctors that specialise in the identification and diagnosis of genetic diseases. Moreover, clinical genetics pertains to the diagnosis, management and counselling of patients affected by genetic conditions, as well as their families.
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.
Clinical Genetic Services - Explaining How We Work
At Genetics.ie, we offer a wide range of genetic testing services for all manner of requirements, covering newborn screening, chromosomal testing and diagnostics to our patients. Our approach focuses on a commitment to the highest standards of patient care and excellent communication throughout.
In this article, we provide an overview of how we work, so that you know precisely what to expect when engaging with our testing services. We understand that these matters are often stressful and worrying, however, we will do our utmost to make the whole process as painless as possible.
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.
Do I Need Carrier Testing for Cystic Fibrosis? What You Should Know
Cystic fibrosis (CF) is a serious inherited disease that leads to problems with food digestion and respiration due to the sticky mucus that builds up the intestines and lungs. It’s a particular worry for parents who are rightly concerned about passing the condition on to their children - something that carrier testing (a.k.a. gene testing) can help with.
Genetic Testing & Why the Information it Provides Is Vital
Found within the strands of your unique DNA are genes, which are passed down to you by your parents, playing a central role in how your body regulates and grows. However, when these genes result in abnormality, the natural consequence of which is a genetic disease.