Select the donor most compatible

with your patient

GENES4LIFE

Genes4Life is a genetic test that is used to investigate whether there is a risk of having a child with an inherited genetic disease. Hereditary diseases are inherited through our genetic material, from one generation to the next. In some cases, diseases can “skip” one generation and be inherited in the next; this happens in diseases with recessive inheritance. Recessive inheritance means that a person can carry disease-related mutations without being aware of it.

RECESSIVE GENETIC DISEASE

Two copies of the same mutated gene, one in the mother and one in the father, cause the disease.

Provide knowledge about 482 genes that are related to rare diseases dueto recessive inheritance.

We study more than 100 high-prevalence diseases andmore than 400 low-prevalence diseases.

 

RISK FREE - THE PERFECT MATCH

78 out of 100 cases analyzed in Amplexa with GENES4LIFE were approved for donation.

In 78 of 100 cases studied with GENES4LIFE , 482 genes that are related to rare diseases of recessive inheritance were analyzed and

no mutations were found. Both patient and donor are compatible.

TYPES OF GENETIC DISEASES WE INVESTIGATE WITH GENES4LIFE:


Reference.-

WE NEED A BLOOD OR SALIVA SAMPLE FOR FOR THE TEST



Genetic testing plays an important role in fertility treatments. One of the reasons why fertility treatments may fail is the presence of genetic mutations, that can lead to repeat abortions and unsuccessful treatments.

GET TESTED BEFORE:

  • Trying to get pregnant.
  • Starting an assisted fertilization treatment.
  • Starting a treatment with donor eggs or sperm. Both patient and donor can be healthy carriers of diseases with a genetic mutation in the same gene.

HOW TO DO IT?






Join our network of clinics and offer the best treatment for your patient