The 20 Best PMM2-Congenital Disorder of Glycosylation Doctors Near Me in edison, NJ

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 edison, NJ. 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

    Amarjit K Saini MDoffice

    1931 Oak Tree Road, 
    Edison, NJ 
     (3.2 miles away)
    Languages Spoken:
    English
    Offers Telehealth

    Amarjit Saini is a primary care provider, practicing in Internal Medicine in Edison, New Jersey. Dr. Saini 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 Obesity, Obesity in Children, Maturity Onset Diabetes of the Young, and High Cholesterol.

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

    Hackensack Meridian Health Carrier Clinic

    252 County Road 601, 
    Belle Mead, NJ 
     (13.8 miles away)
    Languages Spoken:
    English
    Offers Telehealth

    Hamid Masood is a primary care provider, practicing in Family Medicine in Belle Mead, New Jersey. Dr. Masood 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 Insomnia, Generalized Anxiety Disorder (GAD), Schizoaffective Disorder, and Familial Hypertension.

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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.

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