Pgdlabs Kuwait

14/09/2025

21/08/2025

🧬 Carrier Exome Testing – Advanced Genetic Screening

Most genetic conditions are passed silently from one generation to the next.
Our Carrier Exome Test uses Next Generation Sequencing (NGS) to study over 3,000 genes linked to recessive and X-linked disorders.

💡 Why it matters:

Consanguinity increases the chance that both partners carry the same mutation.

If both are carriers, the risk of having an affected child rises significantly.

At PGD Labs Kuwait, we provide the latest genetic tools to help families build a healthier future.

🧬 فحص الإكسوم الحامل – فحص جيني متقدم

معظم الأمراض الوراثية تنتقل بصمت من جيل إلى آخر.
يستخدم فحص الإكسوم الحامل لدينا تقنية التسلسل الجيني المتوازي (NGS) لدراسة أكثر من ٣٠٠٠ جين مرتبطة بالأمراض المتنحية و المرتبطة بالكروموسوم X.

💡 لماذا هذا مهم؟

زواج الأقارب يزيد من احتمال أن يحمل الزوجان نفس الطفرة الجينية.

إذا كان كلا الزوجين حاملين، فإن خطر إنجاب طفل مصاب يرتفع بشكل كبير.

في مختبرات PGD الكويت، نوفر أحدث الأدوات الجينية لمساعدة العائلات على بناء مستقبل أكثر صحة.
📲 Contact us today to book your Carrier Exome Test.

+965 969 38400

01/07/2025

“🥦🧬 Boost Male Fertility with Antioxidant Power
Did you know? High s***m DNA fragmentation can reduce fertility — but nutrition can help. The health of your s***m is deeply connected to what you eat. Oxidative stress is a key cause of DNA damage in s***m cells. A diet rich in antioxidants can lower this stress and improve s***m quality.
✅ Top antioxidant-rich foods to improve s***m DNA quality:
🥜 Brazil nuts – selenium
🫐 Blueberries – vitamin C
🥬 Spinach & kale – folate
🐟 Salmon – omega-3
🍫 Dark chocolate – zinc
🍅 Cooked tomatoes – lycopene
🥚 Eggs – vitamin E
🌿 Green tea – catechins
At PGDLabs, we offer the DNA Fragmentation Test to evaluate s***m integrity — a key factor in male fertility and IVF success. 📲 Book now via WhatsApp: +965 9693 8400 💌 info@pgdlabs.com 💚 Because nutrition and science go hand in hand.
***mHealth ***m “🥦🧬 عزّز خصوبتك بالأغذية المضادة للأكسدة
هل تعلم؟ ارتفاع نسبة تفتّت الحمض النووي في الحيوانات المنوية قد يقلل من فرص الإنجاب — لكن التغذية الصحية يمكن أن تساعد. صحة الحيوانات المنوية ترتبط بما نأكله. الإجهاد التأكسدي هو من أهم أسباب تلف الحمض النووي. النظام الغذائي الغني بمضادات الأكسدة يقلل من هذا التلف ويحسن جودة الحيوانات المنوية.
✅ أطعمة غنية بمضادات الأكسدة لتحسين الحمض النووي:
🥜 مكسرات البرازيل – السيلينيوم
🫐 التوت الأزرق – فيتامين C
🥬 السبانخ والكرنب – حمض الفوليك
🐟 السلمون – أوميغا ٣
🍫 شوكولاتة داكنة – الزنك
🍅 طماطم مطبوخة – الليكوبين
🥚 البيض – فيتامين E
🌿 الشاي الأخضر – الكاتيشين
في PGDLabs، نقدم اختبار تفتّت الحمض النووي في الحيوانات المنوية لتقييم سلامة المادة الوراثية — وهو عامل أساسي في خصوبة الرجل ونجاح التلقيح الصناعي. 📲 احجز الآن عبر واتساب: +965 9693 8400 💌 info@pgdlabs.com 💚 التغذية والعلم... وجهان لرحلة الخصوبة.
#الكويت

“

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14/04/2025

“📉 If you’re facing azoos***mia (no s***m) or severe oligozoos***mia (very low s***m count), a genetic cause may be involved.

🔬 The Y chromosome microdeletion test is essential to diagnose these severe forms of male infertility.
It detects missing genetic material that affects s***m production — and helps guide treatment decisions, including IVF strategies.

🧬 A simple blood test. Fast. Non-invasive. High clinical value.

📲 Contact us on WhatsApp: +965 9693 8400
💬 Ask your fertility doctor if this test is right for you.

***mDNA
“📉 إذا كنت تعاني من انعدام النطاف (Azoos***mia) أو قلة النطاف الشديدة (Oligozoos***mia)، فقد يكون السبب وراثيًا.

🔬 اختبار الحذف المجهري في كروموسوم Y ضروري لتشخيص هذه الحالات الشديدة من العقم الذكوري.
يكشف هذا التحليل عن فقدان مواد وراثية تؤثر على إنتاج الحيوانات المنوية — مما يساعد في تحديد خطة العلاج أو استراتيجية أطفال الأنابيب.

🧬 فحص دم بسيط، غير جراحي، وسريع، وله قيمة طبية عالية.

📲 تواصل معنا عبر واتساب: +965 9693 8400
💬 اسأل طبيب الخصوبة إن كان هذا الفحص مناسبًا لك.”

“

09/04/2025

“Even if your semen analysis looks normal, your s***m DNA might not be.
The fragmentation test helps detect hidden DNA damage that affects fertility.

✔️ Non-invasive
✔️ Fast results
✔️ High impact on treatment decisions

📲 Ask your fertility specialist or message us for more info.

***mDNA

“
حتى وإن كانت نتائج تحليل السائل المنوي طبيعية، قد يحتوي الحمض النووي في الحيوانات المنوية على تلف غير مرئي.
اختبار تكسّر الحمض النووي يُظهر هذا الضرر الخفي الذي قد يؤثر على الخصوبة.

✔️ غير جراحي
✔️ نتائج سريعة
✔️ يُساعد في اتخاذ قرارات العلاج الصحيحة

📲 اسأل طبيب الخصوبة أو تواصل معنا لمزيد من المعلومات.”

19/03/2025

NIPT (Non-Invasive Prenatal Test) allows us to determine the risk of chromosome abnormalities that could affect your baby’s health. During pregnancy, the baby's placenta releases small pieces of genetic material (known as DNA) into mother’s blood stream. Only one sample of maternal blood is needed to analyze these DNA fragments and determine if the baby is at risk of having certain chromosomal conditions that could affect its health, along with providing your baby’s gender.
The test can be done after 9 weeks of pregnancy.

Test options at PGDlabs:
1) Baby Gender: Detection of Y chromosome in maternal blood. Presence of Y chromosome is compatible with male fetus while absence with female fetus. This test will not detect chromosome abnormalities.
2) Baby Basic: Detection of extra or missing copies of chromosomes X, Y, 13, 18 and 21. Abnormalities of these chromosomes are the more common. Also provides information about the gender.
3) Baby Advance: Detection of extra or missing copies of ALL chromosomes plus small deletions and duplications related to 10 well-known syndromes. Also provides information about gender.
In case of twin pregnancy, consult with us.
Please contact +969 38 400 for more details!

PGDlabs is a Genetic Center in Kuwait, specialized in Reproductive Genetics. Offering most suitable

27/02/2025

“Find PGDlabs and Get in Touch!
🌟 Looking for Trusted Genetic Testing Services?
PGDlabs is here to help you with all your genetic testing needs, whether it’s for fertility, preconceptional screening, or advanced testing like PGD, NGS, and more.

📍 Where to Find Us:
Visit us at Jabriya Medical Center!
We are located on the 6th floor, Fourth Ring Road, Jabriya Block 1A, Kuwait.

📞 How to Contact Us:
For questions, appointments, or more information, you can reach us easily:
✔️ WhatsApp: +965 969 38 400
✔️ Phone: +965 969 38 400
⏰ Hours of Operation: 9:00 a.m. - 5:00 p.m.
🌐 www.pgdlabs.com

🌟 At PGDlabs, we’re committed to providing you with the best in genetic testing and support every step of the way.

👉 Contact us today and take the first step toward a healthier future!

21/02/2025

“Aneuploidy Testing with PGD and NGS Technology
🔬 What is Aneuploidy Testing?
Aneuploidy refers to the presence of an abnormal number of chromosomes in an embryo, which can lead to conditions such as Down syndrome, Turner syndrome, Klinefelter syndrome, and more. Preimplantation Genetic Diagnosis (PGD) with Next-Generation Sequencing (NGS) allows us to screen embryos for chromosomal abnormalities before implantation, increasing the chances of a healthy pregnancy.

🌟 How is Aneuploidy Testing Performed?
1️⃣ IVF Procedure: Embryos are created through in-vitro fertilization (IVF).
2️⃣ Embryo Biopsy: A few cells are carefully removed from the embryo on day 5 or 6.
3️⃣ NGS Analysis: The DNA from the biopsied cells is sequenced using NGS technology to detect any chromosomal abnormalities (aneuploidies).
4️⃣ Embryo Selection: Only embryos with a normal chromosomal count (euploid) are selected for implantation, improving the chances of a healthy pregnancy and reducing the risk of miscarriage.

💡 Who Can Benefit from Aneuploidy Testing?
✔️ Women of advanced maternal age (over 35), as they have a higher risk of chromosomal abnormalities.
✔️ Couples with a history of miscarriage or failed IVF attempts, often linked to chromosomal issues.
✔️ Couples undergoing IVF who want to improve the chances of a healthy pregnancy.
✔️ Families with a known genetic history of chromosomal disorders (e.g., Down syndrome, Turner syndrome).

🌟 Why is Aneuploidy Testing Important?
Aneuploidy testing helps ensure that only the healthiest embryos are implanted, greatly increasing the likelihood of a successful pregnancy and reducing the risk of genetic conditions.

👉 Ask your fertility doctor about Aneuploidy Testing through PGD with NGS can help you build a healthy family!

”””

17/02/2025

“💡 Did you know?
1 in 4 couples in the Middle East carry a genetic condition without knowing it. Preconception genetic testing can help identify risks early.

🔬 What is Preconception Genetic Testing?
It’s a screening test for couples to detect carrier status for genetic conditions like:
📌 Sickle Cell Anemia
📌 Thalassemia
📌 Cystic Fibrosis
📌 Spinal Muscular Atrophy (SMA)
📌 G6PD Deficiency

🌟 How It Helps:
✔️ Identifies shared risks between partners.
✔️ Guides family planning and reproductive choices.
✔️ Ensures peace of mind for the journey ahead.
💡 Take charge of your family’s future with advanced genetic testing at PGDlabs
“

10/02/2025

“Who Should Consider the S***m FISH Test?
🔬 Is S***m FISH Testing for You?
S***m FISH is a groundbreaking test that uncovers chromosomal abnormalities in s***m. But who benefits most from this test?

👨‍⚕️ Recommended for:
1️⃣ Men with abnormal semen analysis (low count, movility, or morphology).
2️⃣ Couples experiencing recurrent miscarriages.
3️⃣ Unexplained infertility cases with no clear female factor.
4️⃣ History of failed IVF or ICSI cycles.
5️⃣ Men over the age of 40, where s***m quality may decline.

💡 How it Helps:
S***m FISH provides critical insights to guide fertility treatments, reduce risks, and optimize chances of success.
🌟 At PGDlabs, we’re here to help you take the next step with confidence.

👉 Contact us now via WhatsApp to learn more or schedule your test!
⏰ Hours of Operation: 9:00 a.m. - 5:00 p.m.
📞 WhatsApp: +965 969 38 400

👉 DM us to learn more!

***mFISH
“

03/02/2025

“Carrier Screening: The Power of Prevention
Carrier screening is a preconception genetic test that identifies if you and your partner carry the same recessive genetic condition.

🔬 Why is this important?
Recessive diseases only affect a child if both parents are carriers of the same mutation. Some prevalent recessive genetic diseases in the Middle East are Thalassemia, Sickle Cell Anemia, Cystic Fibrosis, Spinal Muscular Atrophy (SMA), G6PD Deficiency, Duchenne Muscular Dystrophy, Autosomal Recessive Polycystic Kidney Disease (ARPKD), Fanconi Anemia, Maple Syrup Urine Disease (MSUD) among others.

💡 Prevention is Key:
✔️ With carrier screening, you can identify risks before starting a family.
✔️ Gain access to life-changing options like IVF with genetic testing.
✔️ Take control of your family’s health journey with informed decisions.

🌟 At PGDlabs, we believe knowledge is power, and prevention is your greatest tool for building a healthy future.
👉 Contact us now via WhatsApp to learn more or schedule your test!
⏰ Hours of Operation: 9:00 a.m. - 5:00 p.m.
📞 WhatsApp: +965 969 38 400

👉 DM us to learn more about carrier screening!

”

28/12/2024

🔬 Discover the cause behind male infertility with advanced genetic testing.
From karyotype analysis to Y-chromosome microdeletion testing, each test provides clear answers to guide the right treatment. 🌟
📞 Trust our experts to take the first step towards parenthood.