• Hereditary Amyloidosis Report - Dante Labs World
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This report does not include the Genome Sequencing test (to be purchased separately)

Panel zur erblichen Amyloidose

Panel zur erblichen Amyloidose

€29.00 EUR
€29.00 EUR
Sale Ausverkauft

✔️ Add-on Report to your Genome Test

Dieses Produkt ist nur für Kunden gedacht, die bereits eines gekauft haben Dante-Genomtest

Hereditäre Amyloidose ist eine Gruppe seltener und systemischer Erkrankungen, die durch die pathologische Ansammlung unlöslicher Proteinfibrillen, sogenannter Amyloide, im Gewebe gekennzeichnet sind. Es gibt verschiedene Arten der hereditären Amyloidose, die sich im zugrunde liegenden genetischen Defekt und im Gewebe unterscheiden, das am stärksten von dieser Ablagerung betroffen ist, die tendenziell die Organfunktionen beeinträchtigt. Es ist möglich, eine erste wichtige Unterscheidung zwischen der hereditären Non-ATTR-Amyloidose und der hereditären Transthyretin-bedingten Amyloidose zu treffen, die wiederum durch Dutzende verschiedener genetischer Mutationen verursacht wird.
Dieser Test unterstützt die Diagnose einer hereditären Amyloidose bei Personen mit einer positiven Familienanamnese der Krankheit und/oder mit darauf zurückzuführenden Symptomen, die sich im Erwachsenenalter tendenziell in Form von Neuropathien, Herzerkrankungen und Nierenerkrankungen manifestieren.

Die Analyse berücksichtigt die Mutation der Keimbahn-DNA und untersucht SNP- und Indel-Mutationen bis zu 150 bp.

  • Verfügbar in weniger als 24 Stunden
  • Basierend auf der Sequenzierung des gesamten Genoms
  • 19 Gene analysiert
  • Untersucht SNP- und Indel-Mutationen bis zu 150 bp

Liste der Hauptbedingungen:
  • Amyloidose, familiäre viszerale Erkrankung
  • Amyloidose, finnischer Typ
  • Primäre kutane Amyloidose
Vollständige Details anzeigen
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    Unlock the power of 100% of your DNA. The genome has 10,000 times more data than most wellness and ancestry DNA test that analyze less than 0.01% of your DNA

Superior Insights

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  • Genetic counseling (extra)
  • Proactive screening report
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Deeper Science

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    We run a clinical multiomics sequencing lab with ISO9001 accreditation and multiple Next Generation Sequencing workflows

10,000 times more data

  • The Dante Genome Test

    Whole genome sequencing is the analysis of your full DNA - 100% of your DNA - the most complete and comprehensive and complex DNA test available.

    We provide whole genome sequencing and generate and analyze 10,000 times more data than traditional genetic tests that only analyze less than 0.01% of your DNA.

  • Traditional DNA Tests

    Traditionally, genetic tests are limited to examining specific genes or regions of the genome, missing more than 99.9% of your DNA.

    These inferior DNA tests are based on an old technology called microarray but provide only limited insights.

FAQ

What is included in the test?

You receive your full whole genome data (FASTQ, BAM and VCF files), and AI reports. You can get additional reports anytime, without the need to re-send your sample.

What is 30X coverage?

30X coverage is the gold standard in clinical grade whole genome sequencing, offering high-confidence variant calls and interpretation. A 30X whole genome is a superior test than a low pass genome or a microarray

Will I get my raw data?

Yes - FASTQ, BAM, and VCF files are included

Who owns my DNA data?

You own your data. 100% of it. 100% of the time.

How do I collect my sample?

You will receive a saliva sample collection kit at home. Painless. Non invasive. Easy to use. And also a prepaid return label to send the sample back to our lab

What about shipping?

Shipping is free. Everywhere in the world. You will receive a return label with your kit to send your sample back to our lab

Do you work with companies?

If you have an interesting project or would like to speak with our B2B Team, please contact us. We provide genomics and multi-omics services to universities, biotech companies, clinics and hospitals