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    Last Updated: 01/09/2026

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    MediFind found 1531 doctor with experience in PMM2-Congenital Disorder of Glycosylation. Of these, 1323 are Experienced, 165 are Advanced, 41 are Distinguished and 2 are Elite.

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    1,531 providers found
      Adel Khdour
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Family Medicine
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Family Medicine

      Aurora Family Medicine

      5333 Douglas Ave, 
      Racine, WI 
      Languages Spoken:
      English, Arabic, German

      Adel Khdour is a primary care provider, practicing in Family Medicine in Racine, Wisconsin. Dr. Khdour is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Familial Hypertension, Hypertension, Glucocorticoid-Remediable Aldosteronism, and Maturity Onset Diabetes of the Young.

      Elite in PMM2-Congenital Disorder of Glycosylation
      Elite in PMM2-Congenital Disorder of Glycosylation
      Madrid, MD, ES 

      Belen Perez practices in Madrid, Spain. Ms. Perez is rated as an Elite expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her top areas of expertise are PMM2-Congenital Disorder of Glycosylation, Propionic Acidemia, Maple Syrup Urine Disease, and SRD5A3-CDG.

      Elite in PMM2-Congenital Disorder of Glycosylation
      Elite in PMM2-Congenital Disorder of Glycosylation

      KU Leuven

      Leuven, VLG, BE 

      Peter Witters-Wang practices in Leuven, Belgium. Witters-Wang is rated as an Elite expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Their top areas of expertise are PMM2-Congenital Disorder of Glycosylation, MPI-CDG, PGM1-CDG, Liver Transplant, and Gastrostomy.

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

      Mountain Region Family Medicine

      444 Clinchfield St, Ste 201-2800, 
      Kingsport, TN 
      Languages Spoken:
      English
      Offers Telehealth

      . Dr. Watson is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Sialic Acid Storage Disease, Sialuria, PMM2-Congenital Disorder of Glycosylation, and Phosphomannoisomerase Deficiency.

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

      Avenues Specialty Clinic - Internal Medicine

      324 East 10th Avenue, Suite 200, 
      Salt Lake City, UT 
      Experience:
      35+ years
      Languages Spoken:
      English, Spanish
      Accepting New Patients
      Offers Telehealth

      Caroline Vargas is a primary care provider, practicing in Internal Medicine in Salt Lake City, Utah. Dr. Vargas has been practicing medicine for over 35 years and is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her top areas of expertise are Autosomal Dominant Hypocalcemia, Phosphomannoisomerase Deficiency, Sialic Acid Storage Disease, and Sialuria. Dr. Vargas is currently accepting new patients.

      William J. Steptoe
      Experienced in PMM2-Congenital Disorder of Glycosylation
      Internal Medicine
      Experienced in PMM2-Congenital Disorder of Glycosylation
      Internal Medicine

      Ballad Health Medical Associates Family Medicine, Internal Medicine And Pediatrics

      2204 Pavilion Drive, Suite 200, 
      Kingsport, TN 
      Languages Spoken:
      English
      Offers Telehealth

      . Dr. Steptoe is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), Glucocorticoid-Remediable Aldosteronism, and Hypertension.

      Hussam Kujok
      Distinguished in PMM2-Congenital Disorder of Glycosylation
      Internal Medicine
      Distinguished in PMM2-Congenital Disorder of Glycosylation
      Internal Medicine

      Hussam Kujok MD

      3609 Mission Ave, Ste A, 
      Carmichael, CA 
      Languages Spoken:
      English
      Accepting New Patients
      Offers Telehealth

      Caring for the whole patient. Internists are equipped to deal with whatever problem a patient brings- no matter how common, rare, simple or complex. They are specially trained to solve puzzling diagnostic problems and can handle severe chronic illnesses and situations where several different illnesses may strike at the same time. Dr. Kujok is rated as a Distinguished provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Sialic Acid Storage Disease, PMM2-Congenital Disorder of Glycosylation, Sialuria, and Phosphomannoisomerase Deficiency.

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

      University Primary Care Practices Inc

      158 W Main Rd, 
      Conneaut, OH 
      Languages Spoken:
      English, Farsi
      Accepting New Patients

      Mehrdad Tavallaee is a primary care provider, practicing in Internal Medicine in Conneaut, Ohio. Dr. Tavallaee is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Glucocorticoid-Remediable Aldosteronism, Hypertension, Familial Hypertension, and Type 2 Diabetes (T2D). Dr. Tavallaee is currently accepting new patients.

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

      University Primary Care Practices Inc

      158 W Main Rd, 
      Conneaut, OH 
      Languages Spoken:
      English, Farsi, Fijian
      Accepting New Patients

      Faranak Zarrabi is a primary care provider, practicing in Internal Medicine in Conneaut, Ohio. Dr. Zarrabi is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her top areas of expertise are Sialuria, Phosphomannoisomerase Deficiency, PMM2-Congenital Disorder of Glycosylation, and Sialic Acid Storage Disease. Dr. Zarrabi is currently accepting new patients.

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

      Michigan Primary Care PLLC

      41400 Dequindre Road, Suite 121, 
      Sterling Heights, MI 
      Experience:
      36+ years
      Languages Spoken:
      English, Polish, Ukrainian
      Accepting New Patients
      Offers Telehealth

      Zbigniew Purzycki is a primary care provider, practicing in Internal Medicine in Sterling Heights, Michigan. Dr. Purzycki has been practicing medicine for over 36 years and is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Hypertension, Familial Hypertension, Glucocorticoid-Remediable Aldosteronism, Ureteroscopy, and Endoscopy. Dr. Purzycki is currently accepting new patients.

      John Burnham
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Family Medicine
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Family Medicine

      Urgent And Outpatient Care, Dover

      110 Dublin Drive, 
      Dover, OH 
      Languages Spoken:
      English

      John Burnham is a primary care provider, practicing in Family Medicine in Dover, Ohio. Dr. Burnham is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Stress Urinary Incontinence, Urinary Incontinence, Glucocorticoid-Remediable Aldosteronism, and Hypertension.

      Nina D. Nayak
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Internal Medicine
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Internal Medicine

      Corewell Health Internal Medicine - 1700 Biddle Ave

      1700 Biddle Avenue, 
      Wyandotte, MI 
      Experience:
      30+ years
      Languages Spoken:
      English, Hindi
      Offers Telehealth

      Nina Nayak is a primary care provider, practicing in Internal Medicine in Wyandotte, Michigan. Dr. Nayak has been practicing medicine for over 30 years and is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her top areas of expertise are High Cholesterol, Hypothyroidism, End-Stage Renal Disease (ESRD), and Hypertension.

      John M. Stafford
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Family Medicine
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Family Medicine

      John M. Stafford And Associates

      3800 Hollywood Road, Suite 101, 
      Saint Joseph, MI 
      Experience:
      47+ years
      Languages Spoken:
      English
      Accepting New Patients
      Offers Telehealth

      John Stafford is a primary care provider, practicing in Family Medicine in Saint Joseph, Michigan. Dr. Stafford has been practicing medicine for over 47 years and is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Sciatica, Scoliosis, PMM2-Congenital Disorder of Glycosylation, and Phosphomannoisomerase Deficiency. Dr. Stafford is currently accepting new patients.

      Matthew G. Lawson
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Family Medicine
      Advanced in PMM2-Congenital Disorder of Glycosylation
      Family Medicine

      Corewell Health Family Medicine - Parkside

      25 South Washington Street, Suite A, 
      Oxford, MI 
      Experience:
      8+ years
      Languages Spoken:
      English
      Offers Telehealth

      Matthew Lawson is a primary care provider, practicing in Family Medicine in Oxford, Michigan. Dr. Lawson has been practicing medicine for over 8 years and is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Familial Hypobetalipoproteinemia, Chorea-Acanthocytosis, Apo A-I Deficiency, and Familial HDL Deficiency.

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

      University Of Cincinnati Physicians Company LLC

      7690 Discovery Dr, 
      West Chester, OH 
      Languages Spoken:
      English
      Accepting New Patients

      Kyle Kaufman is a primary care provider, practicing in Pediatrics and Internal Medicine in West Chester, Ohio. Dr. Kaufman is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Sitosterolemia, Crohn's Disease, Common Cold, and Tracheitis. Dr. Kaufman is currently accepting new patients.

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

      Millennium Physician Group LLC

      938 Oakfield Dr, 
      Brandon, FL 
      Languages Spoken:
      English, Spanish
      Accepting New Patients
      Offers Telehealth

      Jomil Villasmil-Sanchez is a primary care provider, practicing in Family Medicine in Brandon, Florida. Dr. Villasmil-Sanchez is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Glucocorticoid-Remediable Aldosteronism, Hypertension, Familial Hypertension, and Sialuria. Dr. Villasmil-Sanchez is currently accepting new patients.

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

      Arnett Clinic, LLC

      810 S 6th St, 
      Monticello, IN 
      Languages Spoken:
      English, Croatian, Filipino, Romanian, Spanish
      Accepting New Patients

      Julie Becker is a primary care provider, practicing in Family Medicine in Monticello, Indiana. Dr. Becker is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her top areas of expertise are Hypertension, Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, and Diabetic Hyperglycemic Hyperosmolar Syndrome. Dr. Becker is currently accepting new patients.

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

      Texas Health Physicians Group

      7001 Granbury Rd, 
      Fort Worth, TX 
      Languages Spoken:
      English
      Offers Telehealth

      Alfred Hulse is a primary care provider, practicing in Family Medicine in Fort Worth, Texas. Dr. Hulse is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His top areas of expertise are Sitosterolemia, High Cholesterol, Type 2 Diabetes (T2D), and Infant Hyperglycemia.

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

      Holy Cross Hospital Inc

      1100 E Broward Blvd, Holy Cross Medical Group, 
      Ft Lauderdale, FL 
      Languages Spoken:
      English, French, Spanish
      Accepting New Patients
      Offers Telehealth

      Michelle Fiorillo is a primary care provider, practicing in Family Medicine in Ft Lauderdale, Florida. Dr. Fiorillo is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her top areas of expertise are High Cholesterol, Acquired Agranulocytosis, Hypertension, and Familial Hypertension. Dr. Fiorillo is currently accepting new patients.

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

      Sentara Medical Group

      4374 New Town Ave, Suite 200, 
      Williamsburg, VA 
      Languages Spoken:
      English
      Accepting New Patients
      Offers Telehealth

      Janice Langer is a primary care provider, practicing in Family Medicine in Williamsburg, Virginia. Dr. Langer is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. Her top areas of expertise are High Cholesterol, Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, and Hypertension. Dr. Langer is currently accepting new patients.

      Showing 1-20 of 1,531

      Last Updated: 01/09/2026

      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 me?

      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 me?

      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 me?

      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 me?

      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 me?

      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 me?

      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 me?

      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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