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

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

Last Updated: 04/28/2026

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MediFind found 6 doctor with experience in PMM2-Congenital Disorder of Glycosylation near Australia. Of these, 6 are Experienced.

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6 providers found
    Experienced in PMM2-Congenital Disorder of Glycosylation

    David J. Coman
    Experienced in PMM2-Congenital Disorder of Glycosylation

    David J. Coman
    501 Stanley Street, 
    South Brisbane, QLD, AU 

    David Coman practices practicing medicine in South Brisbane, Australia. Mr. Coman 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 Classic Galactosemia, Ataxia-Telangiectasia, Galactokinase Deficiency, and Galactose Epimerase Deficiency.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Wendy E. Heywood
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Wendy E. Heywood
    215 Franklin Street, 
    Melbourne, VIC, AU 

    Wendy Heywood practices practicing medicine in Melbourne, Australia. Ms. Heywood is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses CLN4 Disease, CLN2 Disease, CLN5 Disease, and CLN1 Disease.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Carolyn J. Ellaway
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Carolyn J. Ellaway
    Randwick, NSW, AU 

    Carolyn Ellaway practices practicing medicine in Randwick, Australia. Ms. Ellaway is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Rett Syndrome, Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), Gastrostomy, and Liver Transplant.

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

    Shanti D. Balasubramaniam
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Shanti D. Balasubramaniam
    Roberts Rd, 
    Subiaco, WA, AU 

    Shanti Balasubramaniam practices practicing medicine in Subiaco, Australia. Ms. Balasubramaniam is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 9 other conditions, according to our data. Her clinical expertise encompasses Multiple Carboxylase Deficiency, Holocarboxylase Synthetase Deficiency, Cutis Laxa, and Gerodermia Osteodysplastica.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Joy W. Lee
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Joy W. Lee
    553 St Kilda Road, 
    Melbourne, VIC, AU 

    Joy Lee practices practicing medicine in Melbourne, Australia. Ms. Lee 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 Asthma, Vocal Cord Dysfunction, Eosinophilic Asthma, Meningococcemia, and Endoscopy.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Edwin P. Kirk
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Edwin P. Kirk
    Randwick, NSW, AU 

    Edwin Kirk practices practicing medicine in Randwick, Australia. Mr. Kirk is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Hirsutism in Women, Cantu Syndrome, Periventricular Heterotopia, and Mosaicism.

    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 1-6 of 6

    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 Australia?

    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 Australia?

    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 Australia?

    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 Australia?

    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 Australia?

    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 Australia?

    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 Australia?

    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 Australia?

    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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