Neurological disorders


In addition to the difficulty of clinical diagnosis, there is a high genetic heterogeneity, making it necessary to approach these conditions through the sequential combination of different genetic tests potentially required for each patient.

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Neurological disorders usually present a complex clinical picture and a high genetic heterogeneity. The massive parallel sequencing approach analyses multiple genes in parallel, enabling these technologies to provide a fast, cost-effective diagnosis. Likewise, other approaches may be the tool of choice in certain types of neurological disorders, for example, using triplet expansion analysis when testing for spinocerebellar ataxia.

NIMGenetics has all the necessary tools for the genetic approach to neurological disorders.

Check our range of NGS genetic testing services for neurological conditions here

ExoNIM® Targeted

Discover ExoNIM® Targeted, our exome analysis approach product based on selecting genes associated with the patient's phenotype.

Learn more about ExoNIM® Targeted

ExoNIM® Clinical

Discover ExoNIM® Clinical, our ExoNIM® approach product that focuses on analysing genes with OMIM (Online Mendelian Inheritance in Man) phenotype.

Learn more about ExoNIM® Clinical

NIMSeq®

Discover NIMSeq® our solution for sequencing multiple genes in a single panel, in order to detect point mutations associated with defined disorders.

Learn more about NIMSeq®

OTHER MOLECULAR DIAGNOSTIC TESTS

NIMGenetics offers genetic testing services based on different molecular biology techniques, including MLPA (Multiplex Ligation-dependent Probe Amplification) and TRP-PCR to test for triplet repeat expansions. We also offer specialists massive parallel sequencing and MLPA techniques to detect genetic alterations in the mitochondrial DNA.

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