Blogs
Family Health History: How It Helps Identify Genetic Health Risks
What Is a Family Health History? A family health history is a record of the health conditions, diagnoses, and other significant medical information affecting your
Understanding the Diagnostic Odyssey in Rare Diseases
What Is the Diagnostic Odyssey? The Diagnostic Odyssey describes the often long and challenging journey a patient and their family may experience before receiving an
What Is Karyotyping? Understanding Your Chromosome Test
What Is Karyotyping? Karyotyping is a laboratory test that examines the number, size, and structure of a person’s chromosomes, the thread-like structures within our cells
Genetic Data: What Is Genetic Data and How Is It Used
What Is Genetic Data? Genetic Data refers to information contained within a person’s DNA that can provide insights into their biological characteristics, inherited traits, and
What to Expect When Your Baby in the NICU
Why Might a Baby Be Admitted to the NICU? Learning that your baby in the NICU needs specialist care can feel overwhelming, particularly if it
What Happens at the 20 Week Anomaly Scan?
What Is the 20-Week Anomaly Scan? The 20 Week Anomaly Scan is a routine ultrasound offered during the second trimester of pregnancy, usually between 18
Failure to Thrive in Babies: Causes and When to Seek Help
What Does “Failure to Thrive” Actually Mean? Failure to thrive is a term used to describe a baby or young child who isn’t gaining weight
Autism Assessment: What to Expect and How to Get One
What Is an Autism Assessment? An autism assessment is a thorough evaluation carried out by trained specialists to determine whether someone meets the criteria for
Speech Delay in Toddlers: When Should Parents Worry?
What Counts as Normal Speech Development in Toddlers? Before worrying about speech delay in toddlers, it helps to have a general idea of what typical
