NEWBORN SCREENING
Our NewBorn Screening Test is designed for the earliest and fastest diagnosis of critically ill newborns and children under 24 months in intensive care units (ICU) and presenting with unclear symptomatology which can be part of a genetic conditions.
Do you know
Up to one-third of all babies and children admitted to the ICU have a genetic disease. For many of them early identification can make the difference for their immediate and later health.
NEWBORN SCREENING
Our NewBorn Screening Test is designed for the earliest and fastest diagnosis of critically ill newborns and children under 24 months in intensive care units (ICU) and presenting with unclear symptomatology which can be part of a genetic conditions such like Bleeding diathesis, Blood abnormalities, Bone fragility, Failure to thrive, Heart abnormality/arrhythmia, Hepatospenomegaly, Hypotonia, Ichthyosis/epidermolysis bullosa, Metabolic abnormalities, Microcephaly, Neutropenia, Abnormal newborn screening results, Respiratory failure, Skeletal abnormalities/craniosynostosis, Skin fragility, Unclear seizures and many others.
CentoICU is designed for analysis more than 850 genes associated with over 100 conditions. The list of included genes was developed by expert medical team based on several selection criteria;
- Early onset
- Severe disease
- ICU related symptomatology
- Diseases/syndromes of differential diagnostic value
OUR NEWBORN SCREENING
- Allows clinicians to utilize just one single test to provide an accurate diagnosis of newborn-related diseases.
- Screens newborns for all ACMG-recommended conditions and those nominated for inclusion.
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.
Request a Call Back?
our medical experts are always available for your support before, during and after the analysis.
goanicgeneticlaboratoryservice@gmail.com
+2347068951861