The 20 Best PMM2-Congenital Disorder of Glycosylation Doctors Near Me in Ankara, TR

Find the Top PMM2-Congenital Disorder of Glycosylation Experts and Specialists

Last Updated: 04/28/2026

Save doctors for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Already have a doctor?
Find A Second Opinion

MediFind found 14 doctor with experience in PMM2-Congenital Disorder of Glycosylation near Ankara, TR. Of these, 14 are Experienced.

Location
LocationClose
14 providers found
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Yılmaz Yıldız
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Yılmaz Yıldız
    Ankara, TR 

    Yılmaz Yıldız practices practicing medicine in Ankara, Turkey. Yıldız is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 12 other conditions, according to our data. Their clinical expertise encompasses Glutaric Acidemia Type 2, Phenylketonuria (PKU), Carbamoyl Phosphate Synthetase 1 Deficiency, and Tyrosinemia Type 3.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Cigdem S. Kasapkara
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Cigdem S. Kasapkara
    Ankara, TR 

    Cigdem Kasapkara practices practicing medicine in Ankara, Turkey. Kasapkara is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 19 other conditions, according to our data. Their clinical expertise encompasses Hypotonia, Glycine Encephalopathy, Malonyl-CoA Decarboxylase Deficiency, and Prolidase Deficiency.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ali Dursun
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ali Dursun
    Ankara, TR 

    Ali Dursun practices practicing medicine in Ankara, Turkey. Dursun is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 12 other conditions, according to our data. Their clinical expertise encompasses Inborn Amino Acid Metabolism Disorder, Phenylketonuria (PKU), Propionic Acidemia, and Isovaleric Acidemia.

    Learn about our expert tiers
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Aysegul Tokatlı
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Aysegul Tokatlı
    Ankara, TR 

    Aysegul Tokatlı practices practicing medicine in Ankara, Turkey. Tokatlı is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 11 other conditions, according to our data. Their clinical expertise encompasses Glutaric Acidemia Type 2, Phenylketonuria (PKU), Propionic Acidemia, and Isovaleric Acidemia.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Hatice S. Sivri
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Hatice S. Sivri
    Ankara, TR 

    Hatice Sivri practices practicing medicine in Ankara, Turkey. Ms. Sivri is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Phenylketonuria (PKU), Glutaric Acidemia Type 2, and Mucopolysaccharidoses (MPS).

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Dogus Vuralli
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Dogus Vuralli
    Ankara, TR 

    Dogus Vuralli practices practicing medicine in Ankara, Turkey. Vuralli is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 5 other conditions, according to our data. Their clinical expertise encompasses Precocious Puberty, Infantile Low Calcium Level, Familial Hypopituitarism, and Breast Enlargement In Males.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Mutluay S. Arslan
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Mutluay S. Arslan
    Ankara, TR 

    Mutluay Arslan practices practicing medicine in Ankara, Turkey. Arslan is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Their clinical expertise encompasses Transient Neonatal Diabetes Mellitus, Epilepsy, Congenital Hyperinsulinism, and Mitochondrial Complex V Deficiency.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Turgay Coskun
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Turgay Coskun
    Ankara, TR 

    Turgay Coskun practices practicing medicine in Ankara, Turkey. Coskun is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 17 other conditions, according to our data. Their clinical expertise encompasses Phenylketonuria (PKU), Fucosidosis, Glutaric Acidemia Type 2, Vitrectomy, and Bone Marrow Aspiration.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Alev O. Ozon
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Alev O. Ozon
    Ankara, TR 

    Alev Ozon practices practicing medicine in Ankara, Turkey. Ozon is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 5 other conditions, according to our data. Their clinical expertise encompasses Precocious Puberty, Intersex, Congenital Adrenal Hyperplasia (CAH), and Breast Enlargement In Males.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Deniz Yuksel
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Deniz Yuksel
    Ankara, TR 

    Deniz Yuksel practices practicing medicine in Ankara, Turkey. Yuksel is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 4 other conditions, according to our data. Their clinical expertise encompasses Subacute Sclerosing Panencephalitis, Glycine Encephalopathy, Measles, Encephalitis, and Gastrostomy.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ayfer Alikasifoglu
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ayfer Alikasifoglu
    Ankara, TR 

    Ayfer Alikasifoglu practices practicing medicine in Ankara, Turkey. Alikasifoglu is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 7 other conditions, according to our data. Their clinical expertise encompasses Precocious Puberty, Juvenile Paget's Disease, Intersex, and Breast Enlargement In Males.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Serdar Ceylaner
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Serdar Ceylaner
    Ankara, TR 

    Serdar Ceylaner practices practicing medicine in Ankara, Turkey. Mr. Ceylaner is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 52 other conditions, according to our data. His clinical expertise encompasses Hypotonia, Glucose-Galactose Malabsorption Deficiency, Camptodactyly Syndrome Guadalajara Type 2, Hormone Replacement Therapy (HRT), and Craniectomy.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Nazlı Gonc
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Nazlı Gonc
    Ankara, TR 

    Nazlı Gonc practices practicing medicine in Ankara, Turkey. Gonc is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 2 other conditions, according to our data. Their clinical expertise encompasses Breast Enlargement In Males, 3M Syndrome, Familial Hypopituitarism, and Diabetes Insipidus (DI).

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Mustafa S. Kılıc
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Mustafa S. Kılıc
    Ankara, TR 

    Mustafa Kılıc practices practicing medicine in Ankara, Turkey. Mr. Kılıc is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 6 other conditions, according to our data. His clinical expertise encompasses Fucosidosis, Visceromegaly, Glycine Encephalopathy, and Hypotonia.

    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
    Showing 1-14 of 14

    Last Updated: 04/28/2026

    What is the definition of PMM2-Congenital Disorder of Glycosylation?

    PMM2-congenital disorder of glycosylation (PMM2-CDG, also known as congenital disorder of glycosylation type Ia) is an inherited condition that affects many parts of the body. The type and severity of problems associated with PMM2-CDG vary widely among affected individuals, sometimes even among members of the same family.

    When should I see a PMM2-Congenital Disorder of Glycosylation doctor in Ankara, TR?

    There are various reasons why you may want to see a specialist, such as: 

    • Your primary care provider recommends it. 
    • Your condition requires expert knowledge and specialized care. 
    • Your symptoms persist or worsen despite treatment. 
    • You need specialized testing or procedures. 
    • You want a second opinion.  

    What should I consider when choosing a PMM2-Congenital Disorder of Glycosylation doctor in Ankara, TR?

    It’s important to see a provider with expertise in your specific condition. Each provider profile in MediFind’s doctor database includes information on which conditions they treat, years of experience, research contributions, languages spoken, insurance plans accepted, and more.  

    How do I find the best PMM2-Congenital Disorder of Glycosylation doctor in Ankara, TR?

    You can find a PMM2-Congenital Disorder of Glycosylation doctor in any of the 10 largest U.S. cities by clicking below:

    PMM2-Congenital Disorder of Glycosylation doctor near New York, NY
    PMM2-Congenital Disorder of Glycosylation doctor near Los Angeles, CA
    PMM2-Congenital Disorder of Glycosylation doctor near Chicago, IL
    PMM2-Congenital Disorder of Glycosylation doctor near Houston, TX
    PMM2-Congenital Disorder of Glycosylation doctor near Phoenix, AZ
    PMM2-Congenital Disorder of Glycosylation doctor near Philadelphia, PA
    PMM2-Congenital Disorder of Glycosylation doctor near Atlanta, GA
    PMM2-Congenital Disorder of Glycosylation doctor near Boston, MA
    PMM2-Congenital Disorder of Glycosylation doctor near Dallas, TX
    PMM2-Congenital Disorder of Glycosylation doctor near San Jose, CA

    How does MediFind rank PMM2-Congenital Disorder of Glycosylation doctors in Ankara, TR?

    MediFind’s rankings are based on a variety of data sources, such as the number of articles a doctor has published in medical journals, participation in clinical trials and industry conferences, as well as the number of patients that provider sees for a given condition. Note that MediFind’s provider database is not based on user reviews, and providers do not pay to be included in the database. 

    What types of insurance are accepted by PMM2-Congenital Disorder of Glycosylation doctors in Ankara, TR?

    Most profiles in MediFind’s doctor database include a list of insurance plans accepted by that provider. However, it’s a good idea to contact the provider’s office to make sure they still accept your insurance, then doublecheck by contacting your insurance plan to confirm they’re in network. 

    How can I book an appointment online with a PMM2-Congenital Disorder of Glycosylation doctor in Ankara, TR?

    MediFind offers direct scheduling for certain providers using the “Request Appointment” button on that provider’s profile. If the schedule option is not available for a provider, tap the red “Show Phone Number” button on their profile to get their contact information. If you prefer to find providers who offer online scheduling, select “Schedules online” under the “Availability” category of the filter feature on the left side of the PMM2-Congenital Disorder of Glycosylation doctor search results page. 

    Why is it important to get a second opinion from a different PMM2-Congenital Disorder of Glycosylation doctor?

    Second opinions are an opportunity to confirm a diagnosis and its root cause, learn about alternative treatment options, or simply gain peace of mind. Many people, especially those with serious diagnoses, get second opinions so they can understand all their options and make informed decisions, so don’t hesitate to get one if you have any doubts or need more information or clarification regarding your care. Note that some insurance plans require second opinions, while others don’t cover second opinions, so be sure to confirm with your insurance provider first.   

    How can I prepare for my appointment with a PMM2-Congenital Disorder of Glycosylation doctor in Ankara, TR?

    Prepare for your appointment by gathering the following items: 

    • Copies of medical records (dating back at least one year) 
    • Your medical history, including illnesses, medical conditions, surgeries, and other doctors you see 
    • Family history of disease 
    • List of current prescription drugs, over-the-counter medicines, vitamins, and herbal remedies or supplements including names and doses 
    • Allergies to medications, food, latex, insects, etc.  
    • List of questions and concerns 
    • Your insurance card 

    You might also contact the provider’s office to see if they offer transportation or childcare services or if you’re allowed to bring a loved one for support or to take notes during your visit. 

    What questions should I ask my PMM2-Congenital Disorder of Glycosylation doctor?

    Here are some sample questions: 

    • Can you explain in simple terms what this condition is and how it’s treated? 
    • What symptoms or side effects should I watch for? 
    • What tests will be involved, and when can I expect results? 
    • Are there other specialists I need to see? 
    • What’s the best way to reach you if I have follow-up questions? 

    How can I learn about the latest clinical trials and research advances my PMM2-Congenital Disorder of Glycosylation doctor may know about?

    MediFind’s Clinical Trials tool asks you a series of questions to help you narrow down your search by health condition, age, gender, location, how far you’re willing to travel, and more. Each question you answer filters down the number of trials until you find the ones that are most relevant to you. 

    MediFind’s Latest Advances tool features summaries of recent articles published in medical journals. We use cutting-edge technology to scour medical publication databases for the latest research advancements on any given condition, then we simplify this information in a way that’s useful and easy to understand. 

    Can I filter my search to show male or female PMM2-Congenital Disorder of Glycosylation doctors in Ankara, TR?

    Look for the filter feature on the left side of the PMM2-Congenital Disorder of Glycosylation doctor search results page. Select “Female” or “Male” under the “Gender” category to search for female or male providers exclusively. If the “Any” option is selected, it will pull results for both male and female providers. 

    Can I filter my search to find a PMM2-Congenital Disorder of Glycosylation doctor that offers video calls?

    Look for the filter feature on the left-side of the PMM2-Congenital Disorder of Glycosylation doctor search results page. Select “Offers telehealth visits” under the Availability category to search for providers who offer virtual appointments (video calls). 

    Reviewed on: 11/11/24  

    By: MediFind Medical Staff 

    Read more about our Content Policy.