NIPT Gender is the simplest version of the NonInvasive Prenatal Test (NIPT), designed for parents who primarily want to know their baby’s sex early in pregnancy.
NIPT Basic is the entrylevel NonInvasive Prenatal Test designed to screen for the most common chromosomal conditions in pregnancy.
NIPT Standard is a more comprehensive version of the NonInvasive Prenatal Test, designed for parents who want deeper insights into their baby’s chromosomal health.
NIPT Plus is an advanced version of the NonInvasive Prenatal Test (NIPT) designed to give expecting parents the most comprehensive view of their baby’s chromosomal health.
Covers breast, ovarian, colorectal, prostate, pancreatic, gastric, melanoma, endocrine, and more.
BRCA1/2 and related genes for breast and ovarian cancer risk.
Genes linked to inherited prostate cancer risk.
Genes associated with inherited pancreatic cancer risk.
Genes for Lynch syndrome and other colorectal risks.
Understanding your family medical history is one of the most proactive steps you can take to protect your long-term health.
While lifestyle factors like diet and exercise are vital, your hereditary cancer risk, the specific gene mutations passed down through generations, can quietly influence your likelihood of developing certain conditions.
Even if you currently feel healthy, mapping out your lineage can reveal a genetic predisposition to cancer that may not be immediately obvious.
Recognising these patterns early gives you the power to shift from reactive to proactive care.
Complete the Free Family Cancer Risk Assessment Quiz — takes just 1 minute
In Nigeria, there are various familial cancer syndromes that predispose individuals to certain cancers, often at younger ages and across multiple generations. Some of these include Lynch Syndrome, which increases the risk of colorectal, endometrial, ovarian, and other gastrointestinal cancers; Familial Adenomatous Polyposis (FAP), caused by APC mutations and associated with hundreds of colon polyps that almost inevitably progress to colorectal cancer if untreated, as well as increased risks of duodenal, thyroid, pancreatic, and childhood liver cancers; and Li‑Fraumeni Syndrome, linked to TP53 mutations and known for causing early‑onset breast cancer, sarcomas, brain tumors, leukemia, and adrenal cancers.
Other important inherited conditions include Hereditary Breast and Ovarian Cancer Syndrome (HBOC)—driven by BRCA1, BRCA2, and related genes—which raises the risk of breast, ovarian, prostate, and pancreatic cancers; and Birt‑Hogg‑Dubé Syndrome, caused by FLCN mutations and associated with kidney cancers and lung cysts. In addition to these syndromes, there are various germline mutations—such as those in BRCA1, BRCA2, APC, TP53, PALB2, and others—that can be inherited and contribute to cancer risk across families.
By identifying a hidden family cancer risk through your family tree, you gain the clarity needed to pursue targeted genetic testing, personalised early screenings, and informed lifestyle adjustments.
Take Action Now. Don’t leave your health to chance. Complete the Free Family Cancer Risk Assessment to see what your family history reveals. It takes just 1 minute and provides immediate, actionable insights
Many cancers, such as breast, ovarian, colorectal, and prostate cancer, can have a hereditary component. If multiple family members have had cancer, or someone was diagnosed at a younger age than usual, it could indicate a genetic predisposition.
Research from the World Health Organization suggests that early identification of genetic risk factors significantly improves long-term outcomes for many cancer types
Knowing your family history allows doctors to:
By acting on this knowledge, you could detect cancer earlier, when treatment is more effective, or even prevent certain cancers through proactive care.
When reviewing your family medical history, it’s important to consider:
Close relatives with cancer (parents, siblings, children, grandparents, aunts)
Multiple cancers on the same side of the family
Early-onset cancer (diagnosed before age 50)
Rare types of cancers or multiple primary cancers in one person
Patterns like these don’t guarantee you’ll develop cancer, but they signal the need for informed action.
For a clear, simple first step, you can take the Family Cancer Risk Assessment and get immediate guidance.
If your assessment indicates a higher risk, genetic testing can confirm whether you carry specific gene mutations linked to hereditary cancers. At Syndicate Bio, we offer testing options tailored to your family history:
Not sure which test fits your situation? Chat with a specialist on WhatsApp for free personalised guidance: Click the button below to start the conversation.
Even if no one in your family has had cancer, it’s worth taking a few minutes to assess your hereditary risk. With a quick quiz and expert guidance, you can gain clarity, peace of mind, and a proactive care plan
Your family history is a roadmap, not a diagnosis. Early awareness could make a life-saving difference for you and your loved ones.
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