Choroideremia
Choroideremia Table of Contents Introduction Choroideremia represents a form of chorioretinal dystrophy linked to the X chromosome, marked by the
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Our Team
Dr. Mehmet Koc Gynecology and IVF Specialist
Dr. Mehmet Koç, a Gynecology and IVF Specialist, has brought joy to thousands of families through successful in vitro fertilization treatments. His approach, blending modern methods with scientific expertise under the guidance of experienced professionals, significantly increases the success rate and ensures family comfort. Dr. Koç's team also specializes in single gene diseases, helping hundreds of families with genetic challenges to have healthy children. Their dedication and experience shine as a beacon of hope for those dreaming of starting a family, offering not just medical solutions but a pathway to happiness and well-being.
Dr. Ahmet Yesilyurt Genetics Specialist
Dr. Ahmet Yesilyurt, Genetics Specialist, is at the forefront of identifying and addressing single-gene disorders. His commitment to this field has been pivotal in helping families conceive healthy children, overcoming genetic challenges. Dr. Yesilyurt's expertise in detecting and managing these complex disorders has not only brought hope to numerous families but also advanced the realm of genetic medicine. His innovative research and dedication to the science of genetics emphasize his significant role in transforming the lives of those affected by single-gene diseases.
Dr. Umut Can Hasanoglu
Gynecologist
Op. Dr. Umut Can Hasanoglu is known for his dedication to scientific research and keeping abreast of innovations in his field. Furthermore, he is recognized for his patient-centered approach and the special care he extends to his patients, dedicating himself to providing them with the best possible support for their health.
Single Gene Diseases & IVF
Why IVF treatment for single gene disease?
In vitro fertilization (IVF) combined with preimplantation genetic diagnosis (PGD) can be an important option for individuals or couples at risk of passing a single gene disease to their offspring.
How do we do IVF?
In vitro fertilization (IVF) represents a remarkable breakthrough in reproductive technology, offering hope to countless individuals and couples facing fertility challenges. This intricate process involves several key stages, each meticulously designed to enhance the chances of conception.
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Single Gene
Single gene diseases are genetic treatments that occur due to a specific gene defect in DNA. This disease is a hereditary fracture that is usually passed on from family to children. Single gene diseases result in genetic changes that disrupt or are missing the normal ability to produce a protein.
IVF (In Vitro Fertilization)
IVF (In Vitro Fertilization) or in vitro fertilization treatment is an assisted reproductive method used to increase the chances of pregnancy for couples with infertility problems. IVF is a medical procedure in which fertilization takes place outside the body, that is, under laboratory conditions.
Preimplantation Genetic Test (PGT)
Preimplantation Genetic Testing (PGT) is a highly specialized procedure used in conjunction with in vitro fertilization (IVF) to identify genetic defects in embryos before they are implanted in the uterus. This technology is crucial for couples at risk of passing on genetic disorders to their offspring.
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Hunter Syndrome (MPS II)
Hunter Syndrome (MPS II) Table of Contents Alternate Terms for Hunter Syndrome (MPS II) Hunter Syndrome, a medical condition, is
Alport Syndrome
Alport Syndrome Table of Contents Introduction Alport syndrome is a collective term used to describe a group of diverse inherited
Lactose intolerance
Lactose intolerance Table of Contents In vitro fertilization (IVF) and preimplantation genetic testing (PGT) are significant advancements in the realm
Familial hypercholesterolemia (FH)
Familial hypercholesterolemia (FH) Table of Contents Alternative Names Type II hyperlipoproteinemia; Hypercholesterolemic xanthomatosis; Low density lipoprotein receptor mutation Introduction Familial
Tay Sachs Disease
Tay-Sachs Disease Table of Contents Other name for this condition: B variant GM2 gangliosidosis GM2 gangliosidosis, type 1 HexA deficiency
X-linked Ichthyosis
X-linked Ichthyosis Table of Contents Introduction X-linked Ichthyosis is a genetic skin disorder that primarily affects males. This condition stems from
Chronic Granulomatous Disease, X-linked
Chronic Granulomatous Disease, X-linked Table of Contents Other Names for This Condition Autosomal recessive chronic granulomatous disease CGD Granulomatous disease,
Comprehensive Guide to Diagnosing Cystic Fibrosis: Methods and Considerations
Diagnosis Methods for Cystic Fibrosis Cystic fibrosis is diagnosed through a series of tests and evaluations to confirm the presence
Androgenetic Alopecia
Androgenetic Alopecia Table of Contents Introduction Androgenetic alopecia, a prevalent type of hair loss affecting both men and women, manifests
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