The 20 Best PMM2-Congenital Disorder of Glycosylation Doctors in Belgium

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

Last Updated: 04/28/2026

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MediFind found 16 doctor with experience in PMM2-Congenital Disorder of Glycosylation near Belgium. Of these, 10 are Experienced, 3 are Distinguished, 2 are Advanced and 1 are Elite.

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16 providers found
    Elite in PMM2-Congenital Disorder of Glycosylation

    Peter Witters-Wang
    Elite in PMM2-Congenital Disorder of Glycosylation

    Peter Witters-Wang

    KU Leuven

    Leuven, VLG, BE 

    Peter Witters-Wang practices practicing medicine in Leuven, Belgium. Witters-Wang is rated as an Elite 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 PMM2-Congenital Disorder of Glycosylation, PGM1-CDG, MPI-CDG, Liver Transplant, and Gastrostomy.

    Distinguished in PMM2-Congenital Disorder of Glycosylation

    Jaak Jaeken
    Distinguished in PMM2-Congenital Disorder of Glycosylation

    Jaak Jaeken
    Leuven, VLG, BE 

    Jaak Jaeken practices practicing medicine in Leuven, Belgium. Jaeken is rated as a Distinguished 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 PMM2-Congenital Disorder of Glycosylation, RFT1-CDG, DPAGT1-CDG, and MPI-CDG.

    Distinguished in PMM2-Congenital Disorder of Glycosylation

    Gert R. Matthijs
    Distinguished in PMM2-Congenital Disorder of Glycosylation

    Gert R. Matthijs
    Leuven, VLG, BE 

    Gert Matthijs practices practicing medicine in Leuven, Belgium. Matthijs is rated as a Distinguished expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 20 other conditions, according to our data. Their clinical expertise encompasses Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism, TMEM165-CDG, DPAGT1-CDG, and PMM2-Congenital Disorder of Glycosylation.

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

    David M. Cassiman
    Distinguished in PMM2-Congenital Disorder of Glycosylation

    David M. Cassiman

    UZ Leuven

    Leuven, VLG, BE 

    David Cassiman practices practicing medicine in Leuven, Belgium. Mr. Cassiman is rated as a Distinguished expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 41 other conditions, according to our data. His clinical expertise encompasses Enlarged Liver, Hereditary Fructose Intolerance, Hepatocerebral Degeneration, Liver Transplant, and Pancreaticoduodenectomy.

    Advanced in PMM2-Congenital Disorder of Glycosylation

    Bart Ghesquiere
    Advanced in PMM2-Congenital Disorder of Glycosylation

    Bart Ghesquiere
    Leuven, VLG, BE 

    Bart Ghesquiere practices practicing medicine in Leuven, Belgium. Mr. Ghesquiere is rated as an Advanced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses DPAGT1-CDG, PMM2-Congenital Disorder of Glycosylation, PGM1-CDG, Kidney Transplant, and Lung Transplant.

    Advanced in PMM2-Congenital Disorder of Glycosylation

    Daisy Rymen
    Advanced in PMM2-Congenital Disorder of Glycosylation

    Daisy Rymen

    KU Leuven

    Leuven, VLG, BE 

    Daisy Rymen practices practicing medicine in Leuven, Belgium. Ms. Rymen is rated as an Advanced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism, Cholesterol Pneumonia, PMM2-Congenital Disorder of Glycosylation, and Cardiomyopathy Hypogonadism Metabolic Anomalies.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Romain Peanne
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Romain Peanne
    Leuven, VLG, BE 

    Romain Peanne practices practicing medicine in Leuven, Belgium. Mr. Peanne is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His clinical expertise encompasses PMM2-Congenital Disorder of Glycosylation, TMEM165-CDG, Cutis Laxa, and Alpha Mannosidosis.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Wouter Meersseman
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Wouter Meersseman
    Leuven, VLG, BE 

    Wouter Meersseman practices practicing medicine in Leuven, Belgium. Meersseman 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 Acute Intermittent Porphyria, Aspergillosis, Porphyria, PMM2-Congenital Disorder of Glycosylation, and Colonoscopy.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Pieter Vermeersch
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Pieter Vermeersch

    UZ Leuven

    Leuven, VLG, BE 

    Pieter Vermeersch practices practicing medicine in Leuven, Belgium. Mr. Vermeersch is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Variegate Porphyria, Severe Acute Respiratory Syndrome (SARS), Vitamin B12 Deficiency, Hereditary Coproporphyria, and Kidney Transplant.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Jef J. Van Den Eynde
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Jef J. Van Den Eynde
    Leuven, VLG, BE 

    Jef Van Den Eynde practices practicing medicine in Leuven, Belgium. Mr. Van Den Eynde is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 14 other conditions, according to our data. His clinical expertise encompasses Tetralogy of Fallot, Aortic Valve Stenosis, Congenital Coronary Artery Malformation, Heart Bypass Surgery, and Transcatheter Aortic Valve Replacement (TAVR).

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Valerie Race
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Valerie Race
    Leuven, VLG, BE 

    Valerie Race practices practicing medicine in Leuven, Belgium. Ms. Race is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses ALG1-CDG, Hereditary Spastic Paraparesis, Troyer Syndrome, and DPAGT1-CDG.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Emile Van Schaftingen
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Emile Van Schaftingen
    Brussels, BRU, BE 

    Emile Van Schaftingen practices practicing medicine in Brussels, Belgium. Mr. Van Schaftingen is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses L-2-Hydroxyglutaric Aciduria, Von Gierke Disease, Agranulocytosis, and Early Infantile Epileptic Encephalopathy.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Liesbeth Keldermans
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Liesbeth Keldermans

    KU Leuven

    Leuven, VLG, BE 

    Liesbeth Keldermans practices practicing medicine in Leuven, Belgium. Keldermans 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 ALG1-CDG, RFT1-CDG, ALG3-CDG, and DPAGT1-CDG.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Elena N. Levtchenko
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Elena N. Levtchenko
    Leuven, VLG, BE 

    Elena Levtchenko practices practicing medicine in Leuven, Belgium. Ms. Levtchenko is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 31 other conditions, according to our data. Her clinical expertise encompasses Cystinosis, Fanconi Bickel Syndrome, Fanconi Syndrome, Hypophosphatemia, and Kidney Transplant.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ingele Casteels
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ingele Casteels
    Leuven, VLG, BE 

    Ingele Casteels practices practicing medicine in Leuven, Belgium. Casteels is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 8 other conditions, according to our data. Their clinical expertise encompasses Cystinosis, Iridogoniodysgenesis Type 1, Optic Glioma, Vitrectomy, and Trabeculectomy.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Renate Zeevaert
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Renate Zeevaert
    't Hasselt, VLG, BE 

    Renate Zeevaert practices practicing medicine in 't Hasselt, Belgium. Ms. Zeevaert is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her clinical expertise encompasses PGM1-CDG, TMEM165-CDG, PMM2-Congenital Disorder of Glycosylation, and Shingles.

    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 1-16 of 16

    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 Belgium?

    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 Belgium?

    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 Belgium?

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

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    How does MediFind rank PMM2-Congenital Disorder of Glycosylation doctors in Belgium?

    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 Belgium?

    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 Belgium?

    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 Belgium?

    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 Belgium?

    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 

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