Genetic illnesses

Please request a personalized kit for the test.

Obtaining the sample at home.

Any illness having a genetic base can be diagnosed through molecular biology techniques. Previous to that, an assessment of the case and a briefing of the family history are required. Amongst them, we diagnose:

  • Ataxia sieving.
  • Research of the Expansion of Myotonic Dystrophy.
  • Research of the markers for the Duchenne Muscular Dystrophy.
  • Research of the Expansion of Huntington´s Chorea.
  • Research of Marfan’s Syndrome.
  • Research of deafness.

Through a personal consultation with the specialists of our team or through the on-line consultation, service at your disposal, with no need to come to our facilities, we give you a professional answer to your doubts, we inform you about the implications of a certain genetic status and we carry out family researches in order to detect in the earliest way as possible the members affected.

How to send your sample?.


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