Erzurum Regional Training and Research Hospital opened its genetics and cytogenetics laboratories that will serve the subtitle Molekülergenetik services.
Photo Erzurum Regional Training and Research Hospital, disorder occurring in a single gene (mutation) resulting from and identification , early treatment and live with associated hereditary diseases single gene disorders make up the group , abortion , down syndrome, FMF ( Mediterranean anemia) relative in order to prevent discomfort caused by birth defects , such as marriage, founded the early diagnosis and treatment center. Photo Erzurum Regional Training and Research Hospital uzm.dr.ebr from the Genetics Department of Marzioğl doctor Özdemir and Spc Cigdem they have identified the majority of genetic diseases of the patients from the region Almighty Heroes , founded located hereditary diseases in the family through this Laboratory themselves that the same genetic disease carries stated that they can learn in a short time with genetic diagnostic methods .
Established these centers nowadays common in society Mediterranean anemia and carrier screening for specific diseases such as blood disorders such as hemophilia and FMF can be made.
recorded in the genetic disease diagnosis and treatment in recent years, rapid development, although still difficult to treat and covering a long period in the prevention of many genetic diseases before diagnosis birth out as the most effective method attracts . A trait or people with sickness in the family , can learn in a short time in this laboratory that the genetic diagnostic methods that themselves are in the same genetic disease carries it or risk group. Photo uzm.dr.ebr the Marzioğl Özdemir and Spc Cigdem Almighty Heroes of our patients come to us ? Single gene disorders ? accurately called an important part said they have identified mutations .
Dr. Marzioğl özdemir clinic application of the general hospital internal medicine ,, hematology, çocuk.römotoloj and women that come patient outcome orientation of the maternity unit , genetic polikilinig the said also directly can be done in your application. Especially in
family with mother and hereditary diseases father , miscarriage during the pregnancy process never having children or my status, children with congenital deformity or developmental delay in a different excuse for not being told they can make their case in laboratory tests whether the application came to this clinic .