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

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

Last Updated: 04/28/2026

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MediFind found 17 doctor with experience in PMM2-Congenital Disorder of Glycosylation near Netherlands. Of these, 14 are Experienced, 2 are Advanced and 1 are Distinguished.

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17 providers found
    Distinguished in PMM2-Congenital Disorder of Glycosylation

    Dirk J. Lefeber
    Distinguished in PMM2-Congenital Disorder of Glycosylation

    Dirk J. Lefeber
    Nijmegen, GE, NL 

    Dirk Lefeber practices practicing medicine in Nijmegen, Netherlands. Mr. Lefeber is rated as a Distinguished expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 26 other conditions, according to our data. His clinical expertise encompasses PGM1-CDG, PMM2-Congenital Disorder of Glycosylation, DPAGT1-CDG, ALG6-CDG, and Leg or Foot Amputation.

    Advanced in PMM2-Congenital Disorder of Glycosylation

    Irena J. Muffels
    Advanced in PMM2-Congenital Disorder of Glycosylation

    Irena J. Muffels
    Utrecht, UT, NL 

    Irena Muffels practices practicing medicine in Utrecht, Netherlands. Muffels is rated as an Advanced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 1 other condition, according to our data. Their clinical expertise encompasses PMM2-Congenital Disorder of Glycosylation, Generalized Tonic-Clonic Seizure, Common Variable Immune Deficiency, and Seizures.

    Advanced in PMM2-Congenital Disorder of Glycosylation

    Mirian C. Janssen
    Advanced in PMM2-Congenital Disorder of Glycosylation

    Mirian C. Janssen
    Nijmegen, GE, NL 

    Mirian Janssen practices practicing medicine in Nijmegen, Netherlands. Ms. Janssen is rated as an Advanced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 18 other conditions, according to our data. Her clinical expertise encompasses Classic Galactosemia, Ballinger-Wallace Syndrome, MELAS Syndrome, Galactokinase Deficiency, and Kidney Transplant.

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

    Marien I. De Jonge
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Marien I. De Jonge
    Nijmegen, GE, NL 

    Marien De Jonge practices practicing medicine in Nijmegen, Netherlands. Ms. De Jonge 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 Strep Throat, Pertussis, Parainfluenza, H Influenzae Meningitis, and Intrauterine Device Insertion.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Stephane B. Heymans
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Stephane B. Heymans
    Maastricht, LI, NL 

    Stephane Heymans practices practicing medicine in Maastricht, Netherlands. Ms. Heymans is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 14 other conditions, according to our data. Her clinical expertise encompasses Myocarditis, Cardiomyopathy, Dilated Cardiomyopathy (DCM), Heart Failure, and Heart Transplant.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ron A. Wevers
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ron A. Wevers
    Nijmegen, GE, NL 

    Ron Wevers practices practicing medicine in Nijmegen, Netherlands. Mr. Wevers is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 22 other conditions, according to our data. His clinical expertise encompasses Xanthoma, Cerebrotendinous Xanthomatosis, Cutis Laxa, and Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Alexis Brice
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Alexis Brice

    Erasmus MC

    Rotterdam, ZH, NL 

    Alexis Brice practices practicing medicine in Rotterdam, Netherlands. Ms. Brice is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 33 other conditions, according to our data. Her clinical expertise encompasses Acute Cerebellar Ataxia, Spastic Paraplegia Type 7, Spasticity, Paraplegia, and Deep Brain Stimulation.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Paola J. De Haas
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Paola J. De Haas
    Nijmegen, GE, NL 

    Paola De Haas practices practicing medicine in Nijmegen, Netherlands. Ms. De Haas is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her clinical expertise encompasses PMM2-Congenital Disorder of Glycosylation and Pulmonary Tuberculosis.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Lonneke De Boer
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Lonneke De Boer
    Nijmegen, GE, NL 

    Lonneke De Boer practices practicing medicine in Nijmegen, Netherlands. De Boer is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Their clinical expertise encompasses Rhabdomyolysis, Protein Deficiency, Newborn Low Blood Sugar, and Canavan Disease.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Alessandra Cambi
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Alessandra Cambi
    Nijmegen, GE, NL 

    Alessandra Cambi practices practicing medicine in Nijmegen, Netherlands. Ms. Cambi is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her clinical expertise encompasses PMM2-Congenital Disorder of Glycosylation.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Saskia B. Wortmann
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Saskia B. Wortmann
    Nijmegen, GE, NL 

    Saskia Wortmann practices practicing medicine in Nijmegen, Netherlands. Ms. Wortmann is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 29 other conditions, according to our data. Her clinical expertise encompasses Classic Galactosemia, Infantile Neutropenia, Von Gierke Disease, Agranulocytosis, and Bone Marrow Transplant.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Nael N. Kasri
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Nael N. Kasri
    Nijmegen, GE, NL 

    Nael Kasri practices practicing medicine in Nijmegen, Netherlands. Mr. Kasri 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 MELAS Syndrome, Coffin-Siris Syndrome, Epilepsy, and Lactic Acidosis.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Teun M. Gunnewiek-Klein
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Teun M. Gunnewiek-Klein
    Nijmegen, GE, NL 

    Teun Gunnewiek-Klein practices practicing medicine in Nijmegen, Netherlands. Gunnewiek-Klein is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Their clinical expertise encompasses MELAS Syndrome and PMM2-Congenital Disorder of Glycosylation.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Laura A. Tseng
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Laura A. Tseng
    Amsterdam, NH, NL 

    Laura Tseng practices practicing medicine in Amsterdam, Netherlands. Ms. Tseng is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her clinical expertise encompasses Epilepsy, Seizures, Epilepsy in Children, and PMM2-Congenital Disorder of Glycosylation.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ben M. Joosten
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Ben M. Joosten
    Nijmegen, GE, NL 

    Ben Joosten practices practicing medicine in Nijmegen, Netherlands. Mr. Joosten is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His clinical expertise encompasses Hyperthyroidism, Thyroid Nodule, and PMM2-Congenital Disorder of Glycosylation.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Wiljan J. Hendriks
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Wiljan J. Hendriks
    Nijmegen, GE, NL 

    Wiljan Hendriks practices practicing medicine in Nijmegen, Netherlands. Hendriks is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Their clinical expertise encompasses Ichthyosis Vulgaris, Glioma, PMM2-Congenital Disorder of Glycosylation, and Gliomatosis Cerebri.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Hans M. Koenen
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Hans M. Koenen
    Nijmegen, GE, NL 

    Hans Koenen practices practicing medicine in Nijmegen, Netherlands. Mr. Koenen is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His clinical expertise encompasses Psoriasis, Scleroderma, Systemic Sclerosis (SSc), and HIV/AIDS.

    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 1-17 of 17

    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 Netherlands?

    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 Netherlands?

    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 Netherlands?

    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 Netherlands?

    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 Netherlands?

    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 Netherlands?

    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 Netherlands?

    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 Netherlands?

    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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