The 20 Best Methylmalonic Acidemia with Homocystinuria Doctors Near Me in cranberry township, PA

Find the Top Methylmalonic Acidemia with Homocystinuria Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 4 doctor with experience in Methylmalonic Acidemia with Homocystinuria near cranberry township, PA. Of these, 4 are Experienced.

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4 providers found
    Experienced in Methylmalonic Acidemia with Homocystinuria
    Family Medicine
    Experienced in Methylmalonic Acidemia with Homocystinuria
    Family Medicine

    GMA/Schogel And Fardo Family Medicine

    213 Executive Drive, Suite 200, 
    Cranberry Township, PA 
     (0.8 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Barbara Fardo is a primary care provider, practicing in Family Medicine in Cranberry Township, Pennsylvania. Dr. Fardo is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia with Homocystinuria. She is also highly rated in 63 other conditions, according to our data. Her clinical expertise encompasses Infant Hyperglycemia, Gitelman Syndrome, Lung Metastases, Colonoscopy, and Ureteroscopy. Dr. Fardo is board certified in American Board Of Family Medicine. Dr. Fardo is currently accepting new patients.

    Experienced in Methylmalonic Acidemia with Homocystinuria
    Internal Medicine
    Experienced in Methylmalonic Acidemia with Homocystinuria
    Internal Medicine

    GMA/Schogel And Fardo Family Medicine

    213 Executive Drive, Suite 200, 
    Cranberry Township, PA 
     (0.8 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Karen Schogel is a primary care provider, practicing in Internal Medicine in Cranberry Township, Pennsylvania. Dr. Schogel is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia with Homocystinuria. She is also highly rated in 42 other conditions, according to our data. Her clinical expertise encompasses Alpha-1 Antitrypsin Deficiency (AATD), Infant Hyperglycemia, Lung Metastases, Anemia, and Ureteroscopy. Dr. Schogel is currently accepting new patients.

    Experienced in Methylmalonic Acidemia with Homocystinuria
    Internal Medicine
    Experienced in Methylmalonic Acidemia with Homocystinuria
    Internal Medicine

    Office

    213 Executive Dr Ste 240, 
    Cranberry Township, PA 
     (0.8 miles away)
    Languages Spoken:
    English
    Offers Telehealth

    Samuel Stepanow is a primary care provider, practicing in Internal Medicine in Cranberry Township, Pennsylvania. Dr. Stepanow is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia with Homocystinuria. His clinical expertise encompasses Neuronal Intranuclear Inclusion Disease (NIID), Gout, Hypothyroidism, and Enlarged Prostate (BPH).

    Learn about our expert tiers
    Experienced in Methylmalonic Acidemia with Homocystinuria
    Internal Medicine
    Experienced in Methylmalonic Acidemia with Homocystinuria
    Internal Medicine
    3447 Harts Run Rd, Suite C, 
    Glenshaw, PA 
     (14.5 miles away)
    Languages Spoken:
    English

    Valerie Donaldson is a primary care provider, practicing in Internal Medicine in Glenshaw, Pennsylvania. Dr. Donaldson is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia with Homocystinuria. Her clinical expertise encompasses Isolated Hypogonadotropic Hypogonadism, Pediatric Growth Hormone Deficiency, Panhypopituitarism, and Hypogonadism.

    Showing 1-4 of 4

    Last Updated: 09/26/2026

    What is the definition of Methylmalonic Acidemia with Homocystinuria?

    Methylmalonic acidemia with homocystinuria is a disorder in which the body is unable to correctly process certain protein building blocks (amino acids), fat building blocks (fatty acids), and  cholesterol. The body is also unable to convert the amino acid homocysteine to another amino acid, methionine. Individuals with this disorder have a combination of features from two separate conditions, methylmalonic acidemia and homocystinuria. There are several forms of this combined condition, and the different forms have different genetic causes and signs and symptoms. The most common and best understood form, called cblC type (or cobalamin C disease), occurs in about 80 percent of affected individuals.

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