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iVF Riga Genetic laboratory news

We would like to pay attention: The Genetic laboratory of iVF Riga Clinic carries out Preimplantation genetic diagnosis (PGD), or the analysis of monogenic diseases, for the families after genetic examination, in which the hereditary genetic disorder is molecularly confirmed.

iVF Riga Clinic offers Preimplantation genetic diagnosis (PGD) of various confirmed monogenic diseases. Currently we have expertise for the testing of following genetic abnormalities:

  • Huntington’s chorea – mutations in the HTT gene
  • Achondroplasia - mutations in the FGFR3 gene
  • Fragile X chromosome syndrome — mutations in the FMR1 gene
  • Myotubular myopathy – mutations in the MTM1 gene
  • Duchenne and Becker muscular dystrophy – mutations in the DMD gene
  • Thoracic Aortic Dissections – mutations in the ACTA2 gene
  • Ichthyosis - mutations in the ALOX12B gene
  • Neuronal ceroid lipofuscinosis – mutations in the TPP1 gene

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Contact our patient's coordinators!
Jelena Silkalna
Jelena Silkalna
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Zita Gaidule (on maternity leave)
Zita Gaidule (on maternity leave)
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Marina Valetko
Marina Valetko
Contact!

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