• Leigh Syndrome Report - Dante Labs
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Leigh Syndrome Report

Leigh Syndrome Report

€19,00 EUR
€49,00 EUR €19,00 EUR
Sale Sold out

 This product is only meant for customers who already 
purchased a Sequencing Test

The Leigh Syndrome Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Leigh Syndrome, instead of a limited set of genes, like old genetic target panels.

Leigh Syndrome is a severe neurological disorder that usually becomes apparent in the first year of life. This condition is characterized by progressive loss of mental and movement abilities (psychomotor regression) and typically results in death within two to three years, usually due to respiratory failure.

Along with environmental factors, Genetics plays a key role in the regulation of Leigh Syndrome.

 

  • 38 genes analyzed
  • 100% genomic regions covered
  • Intragenic and intergenic regions analyzed
  • All variants reported

 

List of genes:

BCS1L
COX10
COX15
DLAT
DLD
LRPPRC
MT-ATP6
MT-CO3
MT-ND1
MT-ND2
MT-ND3
MT-ND4
MT-ND5
MT-ND6
MT-TI
MT-TK
MT-TL1
MT-TL2
MT-TV
MT TW
PC
PDHA1
PDHB
PDHX
SCN4A
SDHA
SURF1
TACO1
NDUFS3
NDUFS4
NDUFA10
NDUFA2
NDUFS8
NDUFA12
NDUFS7
NDUFV1
SERAC1
SLC19A3

See more about the product

What You Get

  • Wellness Report

    The Wellness Report clarifies which habits are best suited to your genome, with actionable insights to live a better life.

    See a report 

  • Scientific Fitness Report

    The Fitness report gives you actionable advice on training, sports, fitness and physical activity. This will help you develop the right workout for you based on your whole genome.

    See a report 

  • Nutrigenomics Report

    Learn about the relationships between food groups and your genes. Using this report, you can create the most effective and personalized diet with a specialist.

    See a report 

  • Health and Predispositions

    Learn more about your risk to develop +50 diseases and conditions. Start taking a proactive approach to your health with our actionable insights.

    See the report 

How it works

  • 1.

    Using a simple at home blood sample, we can collect the 100% of your DNA and analyze the genetic sequence in our lab.

  • 2.

    The sequence is divided into several parts, amplified, grouped in clusters and then sequenced.

  • 3.

    This sequencing process reveals the order of nucleotides that make up the original DNA sample.

  • 4.

    We then compare the genome with a generic and globally recognized reference DNA sequence.

Simple Blood Sample Collection

Painless, quick at home sample collection. User friendly device with CE-IVD mark and FDA approval.

Simply follow the packaging instructions and send the sample back using the pre-paid returns label.

Genomic Consultation Service

Additional reports

Check out the full range of our additional reports, available upon completion of the Genome Test.

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