The 20 Best PMM2-Congenital Disorder of Glycosylation Doctors Near Me in saint peters, MO

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

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in PMM2-Congenital Disorder of Glycosylation near saint peters, MO. Of these, 2 are Experienced.

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

    Hospital Based Practice

    10 Hospital Dr, 
    Saint Peters, MO 
     (2.7 miles away)
    Languages Spoken:
    English

    John Hartweger is a primary care provider, practicing in Internal Medicine in Saint Peters, Missouri. Dr. Hartweger is rated as an Experienced provider by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 36 other conditions, according to our data. His clinical expertise encompasses Infectious Arthritis, Pneumonia, Multisystem Inflammatory Syndrome in Children (MIS-C), Endoscopy, and Colonoscopy.

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

    Barnes-Jewish St. Peters Hospital

    10 Hospital Dr, 
    Saint Peters, MO 
     (2.7 miles away)
    Languages Spoken:
    English

    Christopher Hill is a primary care provider, practicing in Internal Medicine in Saint Peters, Missouri. Dr. Hill is rated as an Experienced provider 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 Chronic Obstructive Pulmonary Disease (COPD), Alzheimer's Disease, Sepsis, Gastrostomy, and Endoscopy.

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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.