Pseudohypoaldosteronism (PHA)
Pseudohypoaldosteronism (PHA) Table of Contents Pseudohypoaldosteronism (PHA) Overview: Understanding the Disorder Pseudohypoaldosteronism encompasses a range of disorders characterized by resistance
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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.
Services
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.
Blog
Familial hypercholesterolemia (FH)
Familial hypercholesterolemia (FH) Table of Contents Alternative Names Type II hyperlipoproteinemia; Hypercholesterolemic xanthomatosis; Low density lipoprotein receptor mutation Introduction Familial
Gitelman Syndrome
Gitelman Syndrome Table of Contents Other names: Familial hypokalemia-hypomagnesemia Gitelman’s syndrome GS Hypokalemia-hypomagnesemia, primary renotubular, with hypocalciuria Tubular hypomagnesemia-hypokalemia with
Gaucher Disease
Gaucher Disease Table of Contents Other Names Cerebroside lipidosis syndrome Gaucher splenomegaly Gaucher syndrome Gaucher’s disease Gauchers disease GD Glucocerebrosidase
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
Sickle Cell Anemia
Sickle Cell Anemia Table of Contents Introduction Sickle cell anemia is a specific type of inherited blood disorder falling under
Red Green Colourblindness
Red Green Colourblindness Table of Contents INHERITANCE Color vision deficiency typically arises from an inherited condition, meaning it is present
Farber Disease
Farber Disease Table of Contents Other names Acid ceramidase deficiency Farber disease Farber lipogranulomatosis Acylsphingosine deacylase deficiency Ceramidase deficiency Farber-Uzman
Thalassemia
Thalassemia Table of Contents Understanding Thalassemia: Types, Causes, and Symptoms Introduction: Thalassemia, derived from the Greek words “thalassa” (sea) and
Maple Syrup Urine Disease (MSUD)
Maple syrup urine disease (MSUD) Table of Contents Other Names for This Condition BCKD deficiency Branched-chain alpha-keto acid dehydrogenase deficiency
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