Welcome to Progene Laboratory

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Our Mission

We promote delivering effective, efficient and respectful genetic service to patients, clinicians and researchers.

Our Vision

To provide genetic testing services by an Egyptian lab with Egyptian hands focusing on providing the best possible patient care and keeping up with innovative scientific advancements.

Our Values

Honesty, integrity, professionalism, hard work, dedication, team working and achievement.

About Us

Offering a Wide Range of Diagnostics Services.

Progene lab is a specialized lab in diagnosis of all inherited human diseases and genetic disorders by the recent molecular diagnostic techniques. We specialized in providing the diagnostic laboratory services.

Enhance Genetic Research in Egypt

Deliver Accurate Genetic Test

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Our Services

Explore Main Services

Target Variant Confirmation by Sanger Sequencing

For variant target analysis, we offer confirmation of a target variant by Sanger sequencing.

Single Gene Analysis by Next Generation Sequencing (NGS)

We offer genetic analysis for specific genes when there is a high degree of suspicion that the patient’s symptoms are caused by a particular gene.

Gene Panel by Next Generation Sequencing (NGS)

Gene panel testing represents a focused approach to test genes that has been linked to your patient's phenotypes

Whole Exome Sequencing (WES) for Single Proband

WES examines the coding genes with simple blood sample and is carefully analyzed by and interpreted by our highly experienced medical team.

Whole Exome Sequencing (WES) for Trio (3 Members of the Same Family)

It is a comprehensive genetic analysis of the affected proband and their parents in order to report the associated variant and establish if the causative variant is inherited or not.

Prenatal Target Variant Analysis in Chorionic Villi Sample

Chorionic villus sampling (CVS) is a procedure in which small samples of placental tissue are obtained for prenatal diagnosis of target genetic variant

PRADER-WILLI (PW) SYNDROME (MS-MLPA)

Prader–Willi syndrome (PWS) is a multisystem, contiguous gene disorder caused by an absence of paternally expressed genes within the 15q11.2-q13 region. MS-MLPA is one of the molecular techniques used to analyze this syndrome

Genetic Analysis Report for Fragile X Syndrome

Fragile X syndrome is caused by a change to a gene on the X-chromosome called the FMR1 gene.

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Tests

Your Questions, Our Answers

Get Answers for Your Questions!

  • What is genetic testing, and why might I need it?

    Genetic testing is a type of medical test that identifies changes in chromosomes, genes, or proteins. It can be used to confirm or rule out a suspected genetic condition and help determine a person’s chance of developing or passing on a genetic disorder.

  • How do I prepare for a genetic test?

    Preparation for a genetic test can vary depending on the type of test being performed. Generally, it's important to understand the purpose of the test, its benefits, risks, and limitations. Your healthcare provider will provide specific instructions based on the test being conducted.

  • What are the different types of genetic tests available?

    Genetic tests can be categorized into various types, including diagnostic testing, predictive and presymptomatic testing, carrier testing, pharmacogenomic testing, and prenatal testing. Each type serves a unique purpose in evaluating genetic conditions.

  • How accurate are genetic tests?

    The accuracy of genetic tests can vary depending on the type of test and the condition being tested for. It's essential to discuss the accuracy and limitations of a specific test with your healthcare provider or a genetic counselor.

  • What are the potential risks associated with genetic testing?

    While genetic testing is generally safe, there are some risks to consider, such as psychological impact, privacy concerns related to genetic information, and the potential for results to have implications for family members.

  • What factors should I consider before ordering a test?

    Usefulness: Genetic testing is particularly useful for patients who have a family history of inherited disorders.

    Cost: For many patients, affordability is an important consideration and should be factored in to the decision-making process. Costs versus benefits also should be considered.

    Reporting: Reports are returned to the physician who ordered the test and should be interpreted by a health care provider with knowledge of the disease genetics.

  • Can the lab re-analyze the data obtained from the previous analysis?

    Reanalysis can be ordered for tests with an initial negative result or variants of uncertain significance after one year. Significant changes to the patient’s clinical features may require a new test and not be considered reanalysis.

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