Physicians & Clinics

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.

When to Refer

Practical referral scenarios

These are common clinical situations where genetic testing route support may help clarify the next diagnostic step.

01

Developmental Delay

Refer when developmental history, dysmorphic features, seizures, regression, or unexplained findings suggest a possible genetic contribution.

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02

Epilepsy

Genetic testing may support cases with early-onset epilepsy, refractory seizures, syndromic features, or family history.

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03

Autism Spectrum Disorders

Testing may be considered when ASD is associated with developmental delay, seizures, dysmorphism, regression, or family history.

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04

Rare Disease Investigations

For complex, multi-system, or undiagnosed cases where specialized test selection and partner laboratory access may be needed.

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05

Cancer Genetics

Refer when cancer occurs at young age, appears repeatedly in the family, or suggests hereditary cancer risk assessment.

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06

Reproductive Genetics

For carrier screening, recurrent pregnancy loss, consanguinity, family history, or reproductive risk clarification.

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07

Family Variant Testing

When a known familial variant has been identified and targeted testing may help clarify relatives’ risk.

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08

Unclear Test Direction

When the clinical question is clear but the right genetic test, panel, or laboratory route is uncertain.

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?

Need Scientific Input?

Send a brief clinical summary and our team can help clarify the appropriate testing route and sample requirements.

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Referral Workflow

How physicians can refer

A clear route for case discussion, test selection, sample coordination, partner laboratory testing, and follow-up communication where applicable.

01

Share case details

Send the clinical concern, available reports, and referral question.

02

Scientific review

Our team reviews the case and clarifies missing information.

03

Test route confirmed

The appropriate test direction and partner laboratory route are discussed.

04

Sample coordination

Collection and logistics are coordinated based on sample requirements.

05

Partner lab testing

Testing is processed through trusted international partner laboratories.

06

Report and follow-up

The report is delivered with follow-up communication where applicable.

Service Guide

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)
Advanced Sequencing

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)
Advanced Sequencing

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
Targeted Genetic Testing

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
Targeted Genetic Testing

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
Family & Reproductive Genetics

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
Family & Reproductive Genetics

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 Genetics

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
Family & Reproductive Genetics

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
Sample Collection

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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Before Referral

Information to prepare

Preparing the clinical context early helps the scientific team clarify the most relevant testing route and sample requirements.

Institutional Partnerships

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

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.

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