The 20 Best PMM2-Congenital Disorder of Glycosylation Doctors Near Me in Ontario, CA

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 10 doctor with experience in PMM2-Congenital Disorder of Glycosylation near Ontario, CA. Of these, 10 are Experienced.

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

    Dawn Cordeiro
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Dawn Cordeiro
    Toronto, ON, CA 

    Dawn Cordeiro practices practicing medicine in Toronto, Canada. Ms. Cordeiro is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Mitochondrial Complex 2 Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, PMM2-Congenital Disorder of Glycosylation, and Sialuria.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Michael R. Chong
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Michael R. Chong
    1280 Main Street West, 
    Hamilton, ON, CA 

    Michael Chong practices practicing medicine in Hamilton, Canada. Mr. Chong is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His clinical expertise encompasses Stroke, Type 2 Diabetes (T2D), Atherosclerosis, and PMM2-Congenital Disorder of Glycosylation.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Roberto Londono-Mendoza
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Roberto Londono-Mendoza
    Toronto, ON, CA 

    Roberto Londono-Mendoza practices practicing medicine in Toronto, Canada. Mr. Londono-Mendoza is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses CHARGE Syndrome, Ehlers-Danlos Syndrome (EDS), Coloboma, and Nicolaides-Baraitser Syndrome.

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

    Luc L. Mertens
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Luc L. Mertens
    555 University Ave, 
    Toronto, ON, CA 

    Luc Mertens practices practicing medicine in Toronto, Canada. Mr. Mertens is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 27 other conditions, according to our data. His clinical expertise encompasses Tetralogy of Fallot, Atrioventricular Septal Defect, Hypoplastic Left Heart Syndrome (HLHS), Heart Transplant, and Kidney Transplant.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Guillaume Pare
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Guillaume Pare
    1280 Main Street West, 
    Hamilton, ON, CA 

    Guillaume Pare practices practicing medicine in Hamilton, Canada. Mr. Pare is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Floating-Harbor Syndrome, Hyperlipidemia Type 3, Type 2 Diabetes (T2D), Stroke, and Heart Bypass Surgery.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Saadet Mahmutoglu-Mercimek
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Saadet Mahmutoglu-Mercimek
    Toronto, ON, CA 

    Saadet Mahmutoglu-Mercimek practices practicing medicine in Toronto, Canada. Mahmutoglu-Mercimek is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 3 other conditions, according to our data. Their clinical expertise encompasses Guanidinoacetate Methyltransferase Deficiency, Epilepsy in Children, Homocystinuria due to MTHFR Deficiency, and X-Linked Creatine Deficiency.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Mahendranath D. Moharir
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Mahendranath D. Moharir
    Toronto, ON, CA 

    Mahendranath Moharir practices practicing medicine in Toronto, Canada. Moharir 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 Stroke, Thrombophlebitis, Mesenteric Venous Thrombosis, Schizencephaly, and Thrombectomy.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Shalini Bahl
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Shalini Bahl
    Toronto, ON, CA 

    Shalini Bahl practices practicing medicine in Toronto, Canada. Ms. Bahl is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, X-Linked Creatine Deficiency, and Enlarged Liver.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Komudi Siriwardena
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Komudi Siriwardena
    555 University Avenue, 
    Toronto, ON, CA 

    Komudi Siriwardena practices practicing medicine in Toronto, Canada. Siriwardena is rated as an Experienced 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 Phenylketonuria (PKU), Urea Cycle Disorders (UCD), Athetosis, and West Syndrome.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Lianna G. Kyriakopoulou
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Lianna G. Kyriakopoulou
    Toronto, ON, CA 

    Lianna Kyriakopoulou practices practicing medicine in Toronto, Canada. Ms. Kyriakopoulou 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, CLN5 Disease, CLN4 Disease, and CLN3 Disease.

    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 1-10 of 10

    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 Ontario, CA?

    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 Ontario, CA?

    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 Ontario, CA?

    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 Ontario, CA?

    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 Ontario, CA?

    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 Ontario, CA?

    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 Ontario, CA?

    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 Ontario, CA?

    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.