Our Multi-Approach

Metabolic Testing

Combining genetic and biochemical testing to deliver a quick and highly accurate multiomic diagnosis of rare metabolic disorders.

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Our bodies are very sensitive to metabolism

if metabolism process fails, it causes the body to have either much or little of the essential substances needed to stay healthy.

CentoMetabolic MOx

Multiomic panel integrating genetic and biochemical testing in a single solution.

Biochemical testing

to support variant classification, leading to higher diagnostic yields

MOX

for fast and accurate diagnosis of a wide range of inherited metabolic disorders.

Multiomic Approach

206 genes and over 20 enzymes and biomarkers associated with more than 180 IMDs.

Best-in-class medical reports

powered by the world’s largest rare disease-centric Bio/Databank from the leader and trusted partner in rare disease diagnostics

Advanced and sensitive detection of sequence variants

With CentoCard and fast TAT of 15 business days
what you should know about

Metabolic Testing

Inherited metabolic disorders (IMDs) are life-long conditions and patients have a wide range of symptoms and needs. They are debilitating, with phenotypic, biochemical and genetic heterogeneity, frequently leading to prolonged diagnostic odysseys.

Our Metabolic Testing is appropriate for physicians providing diagnoses and treatments for patients matching any of the following criteria:

  • Suspected metabolic disorder
  • Overlapping symptoms and floppy babies
  • Infants with lethargy, abdominal pain, vomiting, jaundice, metabolic acidosis
  • Abnormal newborn screening results
  • Developmental delay
  • Infants admitted to a neonatal intensive care unit (NICU), especially due to epilepsy of unclear origin and disturbed consciousness
  • Symptoms related to neurological conditions of unknown etiology

With our multiomic approach, we can help patients accelerate the critical journey from symptoms to diagnosis by avoiding stepwise testing – saving time, resources, and pivotal years during which IMDs can rapidly progress.

We Offer Superior Services

The choice of the appropriate testing strategy and a quick response are key factors to minimize the stress. We assist you at every step of processing your request.

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More Answers Today. More Options Tomorrow.

With CentoMetabolic MOx we provides you with the most valuable information for diagnosis decisions, prognosis and therapeutic approaches, laying the roadmap to personalized treatment options.

Going Beyond Genetics – with CENTOGENE’s multiomic panel – CentoMetabolic MOx

CentoMetabolic MOx

CENTOGENE’s multiomic panel

CentoMetabolic MOx — has been designed to test for a wide range of IMDs — integrating genetic and biochemical testing in one single solution, for the fast and accurate diagnoses.

CentoMetabolic targets close to 200 genes. The content and design of the panel is based on our continuously enhanced medical expertise and knowledge of rare metabolic disorders, including the latest medical and in-house findings.

CentoMetabolic MOx panel includes biomarkers and enzymatic assays for over 20 metabolic disorders. When genetic variants relevant to a patient are then detected via CentoMetabolic MOx, we automatically complement the analysis with biomarkers and/or enzyme testing if applicable, and include the results in the medical report.

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our medical experts are always available for your support before, during and after the analysis.

goanicgeneticlaboratoryservice@gmail.com

+2347068951861