General Diseases Evaluation Center of Reyap Hospital provides service with physicians who are specialists in their field, advanced technological infrastructure, multidisciplinary approach where all branches exist together, and personalized holistic treatment approach. General Diseases Evaluation Center of Reyap Hospital provides education and genetic counseling to patients who may be in the risk group due to their personal or family history of genetic diseases; performs hereditary disease risk scannings.
In General Diseases Evaluation Center of Reyap Hospital, especially cancer genetic studies are performed. In General Diseases Evaluation Center of Reyap Hospital, targeted cancer treatment which provides the protection of healthy cell is planned in the light of genetic tests, and the risk of developing many cancers can be predicted with the help of genetic tests and precautions can be taken before the disease develops. In addition, genetic counselling studies for future mother and father before pregnancy are among the health services that our patients frequently apply in our center. In our hospital, genetic counselling is also given during pregnancy and studies are performed on childhood genetic disorders.
Genetic tests provide an opportunity to prevent or diagnose diseased genes earlier. The results obtained will help you make informed medical and lifestyle decisions, understand your risk of diseases, and provide useful information to other members of your family.
As Reyap Hospital, we aim to provide respectful, polite and highest quality health care services in a devoted environment. We always welcome you to provide all kind of care by the staff who are experienced in their field.
Our Featured Genetic Diseases Evaluation Center Applications
- Karyotype (Chromosome Analysis)
- Thrombophilia Panel (Factor V Leiden, Factor II “Prothrombin”, Mthfr A1298C, Mthfr C677T)
- Fragile X (Premature Ovarian Insufficiency)
- Array CGH
- Amniocentesis – Cordocentesis
- SMA (SMN1 - SMN2 Genes)
- DMD
- Cystic Fibrosis
- Hereditary Diseases Panel (In Consanguineous Marriages)
- WES (Full Exome)
- Clinical Exome
- NIPT (Chromosome Analysis from Fetal Blood)
- Infertility Panel for Male (AR, CATSPER1, CFTR, FSHR, LHCGR)
- Infertility Panel for Female (FSHB, FSHR, LHB, LHCGR)
- Y Microdeletion
- FMF
- HLA B27
- Celiac HLA DQ2 - DQ8
- HFE
- CMT PMP22
- Other Special Panels and Single Gene Studies
Cancer Scanning
- Hereditary Cancer (Oncological) Genetic Tests
- BRCA 1-2 Gene Mutation Test
- Liquid Biopsy
- All Genome Sequences