The 20 Best PMM2-Congenital Disorder of Glycosylation Doctors Near Me in canton, MI

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

Last Updated: 09/26/2026

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MediFind found 8 doctor with experience in PMM2-Congenital Disorder of Glycosylation near canton, MI. Of these, 6 are Experienced and 2 are Advanced.

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8 providers found
    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine
    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine

    Corewell Health Internal Medicine - 2050 N Haggerty Rd

    2050 North Haggerty Road, Suite 100, 
    Canton, MI 
     (1.3 miles away)
    Languages Spoken:
    English, Hindi, Telugu, Urdu
    Accepting New Patients
    Offers Telehealth

    Indrani Nimmagadda is a primary care provider, practicing in Internal Medicine in Canton, Michigan. Dr. Nimmagadda is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Hypertension, Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, Gastrostomy, and Ureteroscopy. Dr. Nimmagadda is board certified in American Board Of Internal Medicine. Dr. Nimmagadda is currently accepting new patients.

    Advanced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine
    Advanced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine

    Iha Health Services Corp.

    990 W Ann Arbor Trl Ste 208, 
    Plymouth, MI 
     (4.8 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Willard Den Houter is a primary care provider, practicing in Internal Medicine in Plymouth, Michigan. Dr. Den Houter is rated as an Advanced provider 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 PMM2-Congenital Disorder of Glycosylation, Phosphomannoisomerase Deficiency, Sialuria, and Sialic Acid Storage Disease. Dr. Den Houter is currently accepting new patients.

    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine
    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine

    Northville Health Center

    39901 Traditions Dr, Floor 2, 
    Northville, MI 
     (8.3 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Audrey Fan is a primary care provider, practicing in Internal Medicine in Northville, Michigan. Dr. Fan is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Cicatricial Pemphigoid, Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), and Hypertension. Dr. Fan is currently accepting new patients.

    Learn about our expert tiers
    Advanced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine
    Advanced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine

    Office

    15130 Levan Rd Ste 30, 
    Livonia, MI 
     (8.5 miles away)
    Languages Spoken:
    English, Hindi
    Accepting New Patients

    Babubhai Jarodiya is a primary care provider, practicing in Internal Medicine in Livonia, Michigan. Dr. Jarodiya is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 11 other conditions, according to our data. His clinical expertise encompasses Gangrene, Gallbladder Disease, Chronic Kidney Disease, Endoscopy, and Gastrostomy. Dr. Jarodiya is currently accepting new patients.

    Experienced in PMM2-Congenital Disorder of Glycosylation
    Family Medicine
    Experienced in PMM2-Congenital Disorder of Glycosylation
    Family Medicine

    Western Wayne Physicians

    23870 Michigan Avenue, 
    Dearborn, MI 
     (11.1 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    David Dziobak is a primary care provider, practicing in Family Medicine in Dearborn, Michigan. Dr. Dziobak is rated as an Experienced provider 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 Chronic Lymphocytic Leukemia (CLL), Obesity in Children, Tracheitis, and Lung Cancer. Dr. Dziobak is board certified in American Board Of Family Medicine. Dr. Dziobak is currently accepting new patients.

    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine
    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine

    Infinity Primary Care PLLC

    37595 7 Mile Rd Ste 240, 
    Livonia, MI 
     (8.8 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Lisa Harston-Ledoux is a primary care provider, practicing in Internal Medicine in Livonia, Michigan. Dr. Harston-Ledoux is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her clinical expertise encompasses Superior Mesenteric Artery Syndrome (SMAS), Mesenteric Artery Ischemia, Sitosterolemia, and Folate Deficiency. Dr. Harston-Ledoux is currently accepting new patients.

    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine
    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine

    Internal Medicine Of Dearborn

    831 Monroe St, 
    Dearborn, MI 
     (12.4 miles away)
    Languages Spoken:
    English, Hindi
    Accepting New Patients

    Shabana Khan is a primary care provider, practicing in Internal Medicine in Dearborn, Michigan. Dr. Khan is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, Hypertension, Gastrostomy, and Ureteroscopy. Dr. Khan is currently accepting new patients.

    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine
    Experienced in PMM2-Congenital Disorder of Glycosylation
    Internal Medicine

    Ghassan A Atto MD PLLC

    14825 Southfield Road, 
    Allen Park, MI 
     (14.5 miles away)
    Languages Spoken:
    English, Arabic
    Offers Telehealth

    Maath Alani is a primary care provider, practicing in Internal Medicine in Allen Park, Michigan. Dr. Alani is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 117 other conditions, according to our data. His clinical expertise encompasses Glucocorticoid-Remediable Aldosteronism, Hypertension, Familial Hypertension, Gastrostomy, and Endoscopy. Dr. Alani is board certified in American Board Of Internal Medicine.

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    Last Updated: 09/26/2026

    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 near canton, MI?

    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 near canton, MI?

    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 does MediFind rank PMM2-Congenital Disorder of Glycosylation doctors near canton, MI?

    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 near canton, MI?

    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 near canton, MI?

    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 near canton, MI?

    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 near canton, MI?

    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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