The 20 Best PMM2-Congenital Disorder of Glycosylation Doctors Near Me in Missouri, US

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

Last Updated: 04/28/2026

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MediFind found 11 doctor with experience in PMM2-Congenital Disorder of Glycosylation near Missouri, US. Of these, 10 are Experienced and 1 are Advanced.

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11 providers found
    Advanced in PMM2-Congenital Disorder of Glycosylation
    Family Medicine
    Advanced in PMM2-Congenital Disorder of Glycosylation
    Family Medicine

    Clay Platte Family Medicine Clinic

    5501 NW 62nd Ter Ste 100, 
    Kansas City, MO 
    Languages Spoken:
    English

    Adrian Delaney is a primary care provider, practicing in Family Medicine in Kansas City, Missouri. Dr. Delaney is rated as an Advanced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 57 other conditions, according to our data. His clinical expertise encompasses Sitosterolemia, High Cholesterol, Vitamin D Deficiency, and Generalized Anxiety Disorder (GAD).

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

    Mercy Clinic Family Medicine And Pediatrics Scenic

    2716 W Republic Rd, 
    Springfield, MO 
    Languages Spoken:
    English
    Offers Telehealth

    Scott Ellis is a primary care provider, practicing in Family Medicine in Springfield, Missouri. Dr. Ellis is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His clinical expertise encompasses Sialic Acid Storage Disease, Phosphomannoisomerase Deficiency, Sialuria, and PMM2-Congenital Disorder of Glycosylation.

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

    Encompass Medical Group Hickman Mills Clinic

    7201 E 147th St, 
    Grandview, MO 
    Languages Spoken:
    English

    Melanie Smolen is a primary care provider, practicing in Family Medicine in Grandview, Missouri. Dr. Smolen is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Dubin-Johnson Syndrome, Rotor Syndrome, Beryllium Disease, and Obesity.

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

    Mercy Labs South LLC

    10010 Kennerly Rd, 
    Saint Louis, MO 
    Experience:
    10+ years
    Languages Spoken:
    English

    Alexander Vaynman is a primary care provider, practicing in Hospital Medicine in Saint Louis, Missouri. He has been practicing medicine for over 10 years. Dr. Vaynman is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Acute Coronary Syndrome, Sepsis, Acute Cystitis, and Low Sodium Level.

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

    Coxhealth Center Aurora

    106 Commerce Dr, 
    Aurora, MO 
    Languages Spoken:
    English

    J-pia Spruill is a primary care provider, practicing in Family Medicine in Aurora, Missouri. Dr. Spruill is rated as an Experienced provider 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 Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Dubin-Johnson Syndrome, and Rotor Syndrome.

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

    Ferguson Medical Group

    320 N Lincoln St, 
    East Prairie, MO 
    Languages Spoken:
    English

    Jimmy Heath is a primary care provider, practicing in Family Medicine in East Prairie, Missouri. Dr. Heath is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 29 other conditions, according to our data. His clinical expertise encompasses Morning Sickness, Anal Cancer, Type 2 Diabetes (T2D), and Cardiomyopathy.

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

    Golden Valley Memorial Healthcare Clinton Clinic

    1602 N 2nd St, 
    Clinton, MO 
    Languages Spoken:
    English
    Offers Telehealth

    Mark Snell is a primary care provider, practicing in Family Medicine in Clinton, Missouri. Dr. Snell is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 19 other conditions, according to our data. His clinical expertise encompasses Neuroendocrine Tumor, Hypothyroidism, Alzheimer's Disease, and Type 2 Diabetes (T2D).

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

    Theodosia Medical Center LLC

    4900 US Highway 160 Ste 2, 
    Theodosia, MO 
    Languages Spoken:
    English

    Samuel Newton is a primary care provider, practicing in Family Medicine in Theodosia, Missouri. Dr. Newton is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Chronic Cough, Dementia, Maturity Onset Diabetes of the Young, and Chronic Obstructive Pulmonary Disease (COPD).

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

    Family Care North Point B & C

    5210 N Belt Hwy, 
    Saint Joseph, MO 
    Languages Spoken:
    English

    Sarah Wiederholt is a primary care provider, practicing in Family Medicine in Saint Joseph, Missouri. Dr. Wiederholt is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 37 other conditions, according to our data. Her clinical expertise encompasses Torticollis, Idiopathic Hypercalciuria, Familial Hypocalciuric Hypercalcemia Type 1, and Milk-Alkali Syndrome.

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

    Coxhealth-Internal Medicine

    1001 E Primrose St, 
    Springfield, MO 
    Languages Spoken:
    English

    Brad Wiley is a primary care provider, practicing in Internal Medicine in Springfield, Missouri. Dr. Wiley is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Osteoporosis, Postmenopausal Osteoporosis, High Cholesterol, and Infant Hyperglycemia.

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

    Quality Health Care Inc

    330 N State St Ste C, 
    Desloge, MO 
    Languages Spoken:
    English
    Offers Telehealth

    Laurence Lum is a primary care provider, practicing in Family Medicine in Desloge, Missouri. Dr. Lum is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 108 other conditions, according to our data. His clinical expertise encompasses Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), Chronic Obstructive Pulmonary Disease (COPD), and Glucocorticoid-Remediable Aldosteronism.

    Showing 1-11 of 11

    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 Missouri, US?

    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 Missouri, US?

    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 in Missouri, US?

    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 Missouri, US?

    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 Missouri, US?

    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 Missouri, US?

    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 Missouri, US?

    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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