Genetic testing support for complex clinical decisions.
Mass Diagnostics helps physicians, clinics, hospitals, laboratories, and healthcare institutions identify referral situations, choose relevant testing routes, coordinate samples, access partner laboratories, and receive clinical communication support.
Practical referral scenarios
These are common clinical situations where genetic testing route support may help clarify the next diagnostic step.
Developmental Delay
Refer when developmental history, dysmorphic features, seizures, regression, or unexplained findings suggest a possible genetic contribution.
Discuss case →Epilepsy
Genetic testing may support cases with early-onset epilepsy, refractory seizures, syndromic features, or family history.
Discuss case →Autism Spectrum Disorders
Testing may be considered when ASD is associated with developmental delay, seizures, dysmorphism, regression, or family history.
Discuss case →Rare Disease Investigations
For complex, multi-system, or undiagnosed cases where specialized test selection and partner laboratory access may be needed.
Discuss case →Cancer Genetics
Refer when cancer occurs at young age, appears repeatedly in the family, or suggests hereditary cancer risk assessment.
Discuss case →Reproductive Genetics
For carrier screening, recurrent pregnancy loss, consanguinity, family history, or reproductive risk clarification.
Discuss case →Family Variant Testing
When a known familial variant has been identified and targeted testing may help clarify relatives’ risk.
Discuss case →Unclear Test Direction
When the clinical question is clear but the right genetic test, panel, or laboratory route is uncertain.
Discuss case →Need Scientific Input?
Send a brief clinical summary and our team can help clarify the appropriate testing route and sample requirements.
Speak with team →How physicians can refer
A clear route for case discussion, test selection, sample coordination, partner laboratory testing, and follow-up communication where applicable.
Share case details
Send the clinical concern, available reports, and referral question.
Scientific review
Our team reviews the case and clarifies missing information.
Test route confirmed
The appropriate test direction and partner laboratory route are discussed.
Sample coordination
Collection and logistics are coordinated based on sample requirements.
Partner lab testing
Testing is processed through trusted international partner laboratories.
Report and follow-up
The report is delivered with follow-up communication where applicable.
Physician catalogues & requests
Download available catalogues directly, or request the remaining test lists from the Mass Diagnostics scientific team.
General Tests Catalogue
Download the available general tests catalogue for physician review and referral planning.
Download PDF →Reproductive Health Tests
Request reproductive genetics, carrier screening, and pregnancy-related genetic testing information.
Request Catalogue →Oncology Tests
Request hereditary cancer, oncology genetics, and cancer-related testing information.
Request Catalogue →Next Generation Sequencing
Request NGS-related testing information including panels, WES, WGS, and advanced sequencing routes.
Request Catalogue →Other Tests Catalogue
Download the available catalogue for additional testing categories and related diagnostic services.
Download PDF →Referral Form & Sample Requirements
Request the referral form, required case information, and sample requirements by test type or partner laboratory.
Request Forms →Genetic testing services with simple explanations
Browse the main services available through Mass Diagnostics. Each card uses the short explanation added in the service profile to keep the clinical route easy to scan.
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 service details →Information to prepare
Preparing the clinical context early helps the scientific team clarify the most relevant testing route and sample requirements.
Genetic testing support for hospitals, clinics, and medical institutions
Mass Diagnostics can support healthcare institutions that need reliable access to advanced genetic testing, international partner laboratory routes, sample coordination, and scientific communication support.
Sample collection support beyond one location
Mass Diagnostics can coordinate sample collection guidance for physician-referred cases across Egypt and selected Arab countries when available, depending on location, sample requirements, and test type.
Have a case or institution that needs genetic testing support?
Speak with our scientific team about referral workflow, sample requirements, partner laboratory access, institutional contracting, or clinical communication support.