Genetic conditions tested include:
Down's Syndrome (Trisomy 21), Edward's Syndrome (Trisomy 18), and Patau's Syndrome (Trisomy 13).
Sex chromosome aneuploidies: Turner syndrome (Monosomy X), Triple X syndrome (Trisomy X), Klinefelter syndrome (XXY), Jacobs syndrome (XYY), and XXYY syndrome.
Microdeletions: DiGeorge syndrome (22q11.2), 1p36 deletion syndrome, Smith-Magenis syndrome (17p11.2), and Wolf-Hirschhorn syndrome (4p16.3).
100 monogenic disorders such as sickle cell disease, cystic fibrosis, hemophilia, fragile X, and many others.
The test is 100% safe to the mother and child and can be done from 10 weeks of pregnancy.
NIPT Test in Kenya
The SRY Gender Test is a DNA-based test used to determine biological sex by detecting the presence of the SRY gene (Sex-determining Region Y) located on the Y chromosome. This gene plays a key role in male development. If the SRY gene is detected in a DNA sample, the individual is genetically male; if it is absent, the individual is genetically female. The test is performed using a simple DNA sample, such as a cheek swab or blood sample, and provides highly accurate results. Because it analyzes genetic material directly, the SRY gender test is a reliable method for confirming biological sex. This test is commonly used in sports and competitive athletics, particularly in disciplines such as boxing, athletics, and other regulated competitions, where verification of biological sex may be required for eligibility in male or female categories. It can also be used for medical, research, or identity verification purposes where confirmation of genetic sex is necessary.
SRY Gender Test
Monogenic disorder testing is a genetic test that looks for changes in a single gene that can cause an inherited condition. These conditions are passed down from parents to children and include diseases such as sickle cell anaemia, cystic fibrosis, and Huntington’s disease. The test works by examining your DNA to identify specific gene changes that may explain symptoms or show your risk of developing a condition. This type of testing is useful for diagnosing health conditions, confirming a suspected genetic disorder, or checking if someone is a carrier who can pass the condition to their children. It can also help guide treatment and family planning decisions. The test usually requires a simple sample, such as blood or saliva. Results are carefully analyzed by specialists to ensure accuracy. Monogenic disorder testing provides clear and focused answers, making it an important tool in modern genetic healthcare.
Monogenic Disorder Test
Instead of testing one gene at a time, these tests analyze many genes together, making the process faster and more efficient. They are commonly used for conditions like inherited cancers, heart diseases, and other genetic disorders where multiple genes may be involved. These tests help doctors identify the cause of symptoms, confirm a diagnosis, or assess a person’s risk of developing certain diseases. Panel tests can also guide treatment decisions and help families understand inherited risks. The test usually requires a simple sample, such as blood or saliva. Results are reviewed by specialists to ensure they are accurate and meaningful. Panel diagnostic testing provides a comprehensive and practical approach to genetic testing, helping patients get clear answers more quickly.
Genetic Panel Test
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