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Genetic diagnosis

REFERENCE CENTRE IN EUROPE

LabGenetics has a catalog of diseases containing more than 1000 genetic tests, each of which has been optimized and validated by our professionals in our own facilities.

Depending on each pathology, for the diagnosis of hereditary and/or rare diseases, LabGenetics performs different molecular studies: NGS and exomes, complete gene sequencing, analysis of frequent mutations, simultaneous sequencing of several genes, expansions, study of large deletions and duplications by MLPA, study of carriers, etc.

Additionally, for all of them, it is also possible to perform prenatal genetic diagnoses from uncultured fetal cells.

Likewise, LabGenetics is able to offer the genetic diagnosis of hereditary and rare diseases using massive sequencing or NGS (Next Generation Sequencing) technology.

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LabGenetics offers a comprehensive genetic diagnostic service, personalized, flexible to the requirements of health professionals, and continuously introduces new genetic diagnostics of hereditary and rare diseases in its portfolio of services. Our goal is to establish close collaborations that allow us to obtain accurate and appropriate results for each case, as quickly and economically as possible.