Medical Genetic Observation Program
Turkey (05-16 / 12 / 2022)

In our Genetic Diseases Diagnosis Center; The following Prenatal (prenatal) and Postnatal (postnatal) genetic tests are performed for the diagnosis and treatment of all genetic diseases with modern genetic practices.

Prenatal (prenatal):
Diagnosing the genetic disease of the unborn baby (fetus) Prenatal Tests We work from the amniotic fluid circulating in the mother’s blood, Chorionic Villus Cord blood or the DNA of the fetus (baby). We diagnose if he is sick.

If there is a genetic disease in the family, we determine whether there is a genetic disease from a single cell of the embryo consisting of the mother and father and we provide the birth of a healthy embryo (Preimplantation Genetic Diagnosis Embryo Selection).

postpartum (postpartum)
– Outpatient clinic (patient examination) Syndrome/Sick children, finding the mutation they carry, finding the gene related to their genetic diseases, learning which genetic disease their parents have, providing genetic counseling accordingly, risk and embryo selection in their future children

– To detect gene mutations related to genetic diseases, to diagnose and treat the disease and to follow up, to direct patients suitable for gene therapy to relevant clinics.

– Pharmacogenetics. Drugs can have different effects and side effects in each person, and drug resistance can be caused by a defect or deficiency in the person’s genes.

– Bacteria-Virus resistance Some agents that cause disease can acquire resistance as a result of resistance/genetic mutations and we detect these mutations and it is determined that other drugs should be used for resistant bacteria and viruses.

– Infertility (infertility) Genetic diseases and factors that are among the causes of infertility in spouses are investigated.

– Organ Transplant Before the transplantation of organs and tissues such as kidney and bone marrow, donor/recipient tissue compatibility is checked. After the transplant, the success of the transplant is determined by genetic testing.

– Cancers: Recently, Smart Molecular drugs have been developed as a result of researching mutations in cancers. These drugs work for specific mutations and these mutations are screened for patient treatment.

– Familial Cancers: Approximately 10% of cancers are familial. Especially in individuals with breast and bowel cancer, genetic mutations in the family are screened to calculate the risk of developing cancer in the future, and early diagnosis and treatment of the disease is provided.

General information:
– The training will be in English.
– The price includes transportation between the airport and the hotel.
– There are only 2 Empty Seats.
– It is an Observation Training.

History :
05-16 / 12 / 2022
09-20 / 01 / 2023
06-17 / 02 / 2023

Cost :
– 2 Weeks: $2,500.
– 1 Month : $3,000.

How to Apply:
– Please send your CV to our info@parsaglik.com e-mail address.
– Write in the e-mail header: (Medical Genetic Observation Program).
– Note: You must submit 10% of the fees within the application deadline to confirm your place.
– We will send you an Invitation letter for visa application.

Accomodation :
– Local 4-star hotel accommodation available for those in need, 40 per day including breakfast