I need help with genetic testing.
Start with the reason you are here. You do not need to know the test name. Mass Diagnostics helps you understand whether genetic testing may help, what information is needed, and what the next step looks like.
Choose the situation closest to yours
These patient journeys are built around real concerns, not complicated test names.
My child has developmental delay or unexplained symptoms
If your child has delayed milestones, seizures, learning difficulties, autism features, or symptoms no one has explained yet, genetics may be one part of the answer.
Open this path → 02We are planning a pregnancy
If you are planning a pregnancy or your doctor recommended carrier screening, genetic testing can help clarify inherited risk before important decisions.
Open this path → 03There is a genetic condition in my family
If a relative has a known genetic condition or variant, family testing may help clarify who else may be affected or at risk.
Open this path → 04I have a family history of cancer
If cancer appears repeatedly in your family or occurred at a young age, hereditary cancer testing may help guide prevention and family conversations.
Open this path → 05I am not sure which test I need
If you have a referral, symptoms, or family history but do not know the test name, start here. We help route the question.
Open this path → ?I want to speak to someone first
Send a short summary of your concern. The team can help you understand the best starting point without needing to choose a test alone.
Ask for guidance →Genetic testing services explained simply
Explore the main genetic testing services available through Mass Diagnostics, each explained in simple language to help you understand when it may be relevant.
Whole Exome Sequencing (WES)
Whole Exome Sequencing (WES) is an advanced genetic test that analyzes the protein-coding regions of the genome to help investigate unexplained symptoms, rare diseases,...
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Whole Genome Sequencing (WGS)
Whole Genome Sequencing (WGS) analyzes nearly all genetic material to provide a comprehensive view of the genome for complex diagnostic investigations and unresolved medical...
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Single Gene Sequencing
Single Gene Sequencing focuses on analyzing a specific gene when clinical findings strongly suggest a particular inherited condition.
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Specific Panels
Specific Panels analyze a selected group of genes associated with a particular disease, symptom, or clinical specialty, providing a focused and efficient testing approach.
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Familial Variant Test
Familial Variant Testing helps determine whether relatives carry a previously identified genetic variant that has already been detected within the family.
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Reproductive Carrier Screening
Reproductive Carrier Screening helps identify whether prospective parents carry genetic variants associated with inherited conditions that could be passed to their children.
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Cancer Carrier Screen Test
Cancer Carrier Screening helps identify inherited genetic variants associated with an increased risk of developing certain types of cancer.
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Proactive Carrier Screen Test
Proactive Carrier Screening helps healthy individuals identify inherited genetic risks before symptoms appear, supporting informed healthcare and family planning decisions.
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Sample Collection Coordination
Mass Diagnostics provides sample collection coordination and logistics support to help patients and physicians access advanced genetic testing services through trusted international laboratory partners.
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تحليل الإكسوم الكامل WES
تحليل الإكسوم الكامل هو فحص جيني متقدم يركز على الأجزاء المسؤولة عن تكوين البروتينات داخل الجينات، وهي المناطق التي ترتبط بعدد كبير من الأمراض...
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تحليل الجينوم الكامل WGS
تحليل الجينوم الكامل هو فحص جيني واسع يقرأ الجينوم بشكل أشمل من فحوصات أخرى، وقد يساعد في الحالات المعقدة أو غير المشخّصة عندما لا...
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تحليل جين واحد
تحليل جين واحد هو فحص جيني يركز على جين محدد عندما يكون الطبيب أو التقرير الطبي لديه اشتباه واضح في جين معين مرتبط بالحالة....
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تحليل لوحات جينية محددة
تحليل اللوحات الجينية المحددة هو فحص يركز على مجموعة مختارة من الجينات المرتبطة بحالة طبية أو سؤال إكلينيكي معين. قد يكون مناسبًا عندما تكون...
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تحليل الطفرة العائلية المعروفة
تحليل الطفرة العائلية المعروفة هو فحص جيني موجّه يُستخدم عندما تكون هناك طفرة أو تغيّر جيني محدد تم اكتشافه سابقًا في أحد أفراد العائلة....
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فحص حاملي الأمراض الوراثية قبل أو حول الحمل
فحص حاملي الأمراض الوراثية هو فحص جيني يساعد الأزواج على معرفة ما إذا كان أحدهما أو كلاهما يحمل تغيّرات جينية قد تزيد احتمال انتقال...
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فحص القابلية الوراثية للإصابة بالسرطان
فحص القابلية الوراثية للإصابة بالسرطان هو فحص جيني يساعد في تقييم ما إذا كان لدى الشخص تغيّرات جينية موروثة قد تزيد احتمالية الإصابة بأنواع...
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فحص حاملي الأمراض الوراثية الموسّع
فحص حاملي الأمراض الوراثية الموسّع هو فحص جيني يهدف إلى تقييم ما إذا كان الشخص يحمل تغيّرات جينية مرتبطة بعدد من الأمراض الوراثية، حتى...
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تنسيق جمع العينات
خدمة تنسيق جمع العينات تساعد المرضى والأطباء في معرفة نوع العينة المطلوبة، طريقة التحضير، والمكان أو الفرع المناسب لجمع العينة قبل إرسالها إلى المعمل...
View simple service explanation →A guided path from concern to next step
Our role is to make the process clearer, especially when the test names feel complicated.
Share your concern
Send your symptoms, referral, family history, or medical question.
Understand the route
We help clarify whether a genetic testing pathway may be relevant.
Prepare requirements
Sample type, documents, and instructions are explained clearly.
Testing coordination
Testing is coordinated through trusted international partner laboratories.
Report support
You receive the report with support around next discussion points.
Sample collection support beyond one location
Mass Diagnostics can coordinate sample collection guidance for patients and physician-referred cases across Egypt and selected Arab countries when available, depending on location, sample requirements, and test type.
Not sure which path fits?
Send a short summary. You do not have to choose the genetic test alone.