Pregnancy is an exciting period in a woman's life that requires her to take special
responsibility and a serious attitude towards her health. To keep the situation under control
and take timely measures to eliminate possible complications, physicians have established an
antenatal care protocol for pregnant women, defined a list of necessary examinations, and
recommendations.
Pregnancy Monitoring involves regular consultations with a doctor, monitoring the
development of the fetus and the health status of the expectant mother, as well as conducting
necessary tests and examinations. Proper antenatal care helps to identify potential
complications promptly, minimize risks, and prepare the woman for childbirth.
Screening tests performed during pregnancy allow us to gain early information regarding the
baby's health. These tests are of great importance for the early diagnosis of congenital
anomalies and chromosomal disorders.
The Non-Invasive Prenatal Test (NIPT) is a blood test that screens for fetal genetic
anomalies by analyzing small fragments of fetal DNA found in the mother's bloodstream.
This test is typically performed after 10 weeks of gestation and is used to assess the risk of
certain genetic conditions, notably Down syndrome (Trisomy 21), Edwards syndrome
(Trisomy 18), and Patau syndrome (Trisomy 13), and other genetic abnormalities. The results
are highly accurate, typically providing 99% accuracy in detecting Down syndrome and other
common chromosomal disorders.
The Double Screening Test is a non-invasive test used to detect chromosomal anomalies at
an early stage, specifically Down syndrome (Trisomy 21) and Edwards syndrome (Trisomy
18). The test is based on two main parameters: maternal blood biochemical analyses and
ultrasound measurements. The Double Screening Test is typically performed between the
11th and 14th weeks of pregnancy.
The Quad Screening Test for the second trimester of pregnancy is a screening examination
performed between 15 and 20 weeks of gestation. It measures the levels of three distinct
substances in the mother's blood: human chorionic gonadotropin (hCG), alpha-fetoprotein (AFP), and unconjugated estriol (uE3), and inhibin A. These markers are utilized to assess the risk of certain chromosomal anomalies and neural tube defects in the fetus.
The Detailed Fetal Ultrasound is performed at 18–22 weeks of gestation to rule out
congenital malformations. The specialist meticulously examines all the organs, assessing
their structure and development. Additionally, the examination evaluates the condition of the
placenta, the amount of amniotic fluid, and measures the fetal size. The procedure typically
lasts approximately 40-60 minutes and provides comprehensive information regarding the
baby's health.
Screening and Tests during pregnancy represent a series of vital examination methods. They
enable the early detection of fetal developmental anomalies and the presence of chromosomal
disorders (such as Down syndrome or Patau syndrome), and they allow the physician to
monitor the health of both the expectant mother and the baby throughout the entire gestation
period.
Our clinic's location in the Famagusta (Gazimağusa), Glapsides region of Northern Cyprus puts you within easy reach of the area's best swimming beaches, restaurants, and resorts, allowing you to relax and unwind during your stay.
Located in Northern Cyprus, this is the most convenient option and is only a 40-minute drive from our clinic.
Located in the South of Cyprus, this is another popular option depending on your passport and flight availability.
To ensure your experience is completely stress-free from the moment you book your flights, your dedicated Patient Coordinator will manage all of your logistical arrangements. We handle every detail so you can focus on your treatment.
We will arrange for a driver to meet you upon arrival and transport you directly to your accommodation and appointments.
We can recommend and assist with booking your stay from a wide range of high-quality hotels, apartments, and boutique options that meet our standards for comfort and convenience.
From your arrival until your departure, we ensure every detail of your visit is thoughtfully managed.
Simply share your travel plans with your coordinator, and we will handle the rest.
For patients requiring an egg or sperm donor, we have a comprehensive and carefully managed donor programme. The process is governed by strict local regulations that ensure complete donor anonymity.
Our donors undergo rigorous screening, including extensive medical, genetic, and psychological evaluations, to ensure the highest standards of quality and safety. While the donor's identity remains anonymous, you will be provided with a detailed, non-identifying profile which typically includes:
This allows you to choose a donor with characteristics that are important to you while respecting the legal framework of anonymity.
We specialize in making the process seamless for our international patients. Your journey is managed by a dedicated International Patient Coordinator who will be your single point of contact.
After your initial consultation, we will create your bespoke treatment plan.
We offer two flexible pathways for our patients travelling from abroad.
For your convenience, you can begin the initial stages of your treatment at home. We will coordinate with a UK-based clinic for your preliminary scans and tests. You then travel to Cyprus to complete the final stages, requiring a stay of as little as one week for your key procedures. This option is popular as it minimizes your time away from home.
Alternatively, you can choose to undertake your entire treatment cycle with us in Cyprus. This allows you to step away from daily routines and relax in our calm, supportive environment. This all-inclusive pathway typically requires a stay of approximately three weeks.
Whichever pathway you choose, your coordinator will assist with planning your trip, providing recommendations for premium accommodation and organizing private airport transfers. Our goal is to manage all the logistics, allowing you to focus completely on your treatment in a calm, stress-free environment.
This is often the first and most important question we receive. While we are proud of our excellent success rates, which are in line with top European clinics, we believe in providing you with a transparent and realistic perspective. Rather than focusing on a single, generic statistic, we provide a personalized success projection during your initial consultation. This is based on your specific age, medical history, and diagnosis.
Our success is built upon the expertise of our world-class clinicians and embryologists, who utilize state-of-the-art laboratory technology, including AI-driven embryo selection. We are committed to ethical and transparent reporting, ensuring you have the confidence and clarity you need to make an informed decision.
