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All of our diagnostic services are already available to you, it is only our webpage that is still in-progess. You can find details on our services through our WEBPORTAL. Login to see our complete list of diagnostic services. If you are not currently a WEBPORTAL user, you can register for free here.

Discover our services

* These services are only available to physicians.

Diagnostic Services for
Rare Diseases

Proven and certified diagnostic services delivering reliable results for Rare Disease diagnosis using advanced analytical techniques including enzyme, biomarker, and genetic testing.

Premium diagnostic services for Rare Diseases.
From enzyme and biomarker to genetic confirmation.

How we help you diagnose Rare Diseases

Path to Rare Disease Diagnosis

*  When available, we perform a biochemical pre-test consisting of an enzyme test and/or a biomarker test.

Rare Diseases

One Rare Disease may affect only a handful of patients, and another may touch thousands. More than 30 million people are affected.
50% of Rare Diseases affect children.

Over 6,000 Rare Diseases are characterized by a broad diversity of disorders and symptoms that vary not only from disease to disease but also from patient to patient suffering from the same disease. Relatively common symptoms can hide underlying rare diseases leading to misdiagnosis and delaying treatment. Rare Diseases are often substantially disabling. The patients quality of life is affected by the lack or loss of autonomy due to the chronic, progressive, degenerative, and frequently life-threatening aspects of the disease.

The fact that there are often no existing effective cures adds to the high level of pain and suffering endured by patients and their families.

Our diagnostic services help to improve diagnosis, chance for treatment and to help families, including their children, obtain fast and reliable diagnosis.

About our Rare Disease Diagnostics

What can cause a Rare Disease?

Nearly 80% of rare diseases have been identified with genetic origins while others result from infections (bacterial or viral), allergies and environmental causes.

Why is it so important to think of Rare Diseases?

Rare Diseases should be included in differential diagnosis of many common diseases. Often not recognized, patients may suffer over many years until a diagnosis is made. Fortunately, many physicians are now aware of these diseases, and we assist and support them by delivering enzymatic, biomarker and/or genetic results.


“Our commitment: improving health through better, faster and earlier diagnosis giving the best chance for treatment and best clinical outcomes.”

More questions about Rare Diseases
and supporting diagnostics?

How to Order Diagnostic Services for Rare Diseases

ARCHIMEDlife Sampling Kit

Our Diagnostic Services for Rare Diseases include comprehensive options for biochemical and genetic testing. Additionally you can choose complete panel diagnostic programs with combined enzyme testing, biomarker testing, and genetic confirmation using full gene sequencing.

All of our services are available to any interested physician or healthcare professional worldwide.

As part of our diagnostic services, we supply complimentary ARCHIMEDlife sampling kits. You can order your sampling kits and diagnostic services though our easy and secure WEBPORTAL and receive your electronic medical report in five simple steps.

Five Simple Steps

1Order Sampling Kit

2Collect the Sample

3Register the DBS card

4Return the Sample

5Receive your Report

More questions about Rare Disease
and supporting diagnostics?


Diagnostics ・Clinical Studies・Patients´Care