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Rare Diseases

BluePrint Multi-Gene Panel

BluePrint offers a wide variety of multi-gene panels focused on diverse areas of study, including cardiology, pulmonology, ophthalmology, pediatrics, neurology, dermatology, endocrinology, immunology, nephrology, and hematology.

Overview

It is estimated that approximately 70,000 people worldwide are affected by the CFTR gene mutation that causes Cystic Fibrosis.

1 in 27 Ashkenazi Jews is a carrier of the Tay-Sachs mutation, a fatal neurodegenerative disorder caused by the absence of an enzyme necessary for breaking down fatty substances in the brain.

5% to 10% of rare genetic diseases have some form of effective treatment available.

Source: 2020 NORD (National Organization for Rare Disorders) Report.

When Should You Consider This Test?

Consider this test in the following cases:

Family History of Genetic Diseases
Diseases of Unknown Cause
Complex Genetic Conditions
Severe or Early-Onset Diseases
Pre-Conception and Prenatal Diagnoses
Personalized Monitoring and Treatment

Genes Analyzed

The panel includes:

Up to

3000

Genes

There are more than 220 panels covering 14 medical specialties, with panels ranging from 2 genes to 3000 genes, depending on the selected panel.

Methodology

The methodology used for this test is as follows:

Sample:

Blood
Saliva

PREPARATION:

Blood: No fasting required.

Saliva: 30 minutes of total fasting.

TURNAROUND TIME:

Up to 21 calendar days.

REQUIRED DOCUMENTS:

Medical request.

Type Description
Technique NGS + CNVs
Depth >100x
Coverage >99% of target regions
VuS Resolution Sanger, MLPA

How to Request the Test?

Contact Our Customer Services
Exatus Gene will send a collection kit and provide instructions for sample collection.
We will retrieve the collected sample and send it to the laboratory for analysis.
The report will be made available through the SysGene Portal and sent to your email.