The 20 Best Isovaleric Acidemia Doctors Near Me in Boston, MA

Find the Top Isovaleric Acidemia Experts and Specialists

Last Updated: 06/30/2026

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MediFind found 2 doctor with experience in Isovaleric Acidemia near Boston, MA. Of these, 2 are Experienced.

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2 providers found
    Experienced in Isovaleric Acidemia

    Dr. Yuval E. Landau
    Medical Genetics
    Experienced in Isovaleric Acidemia

    Dr. Yuval E. Landau
    Medical Genetics
    Referral may be required
    80 Pleasant St, Apt #51, 
    Brookline, MA 
    617-383-4190
    Languages Spoken:
    English

    Yuval Landau is a Medical Genetics provider practicing medicine in Brookline, Massachusetts. Dr. Landau is rated as an Experienced provider by MediFind in the treatment of Isovaleric Acidemia. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Orotic Aciduria Type 1, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Urea Cycle Disorders (UCD).

    Experienced in Isovaleric Acidemia
    Experienced in Isovaleric Acidemia
    Referral may be required

    Cra Danvers Imaging LLC

    102 Endicott St, 
    Danvers, MA 
    978-882-6191
    Languages Spoken:
    English
    See accepted insurances

    Mark Anderson is a Cardiologist practicing medicine in Danvers, Massachusetts. Dr. Anderson is rated as an Experienced provider by MediFind in the treatment of Isovaleric Acidemia. He is also highly rated in 25 other conditions, according to our data. His clinical expertise encompasses Arrhythmias, Atrial Fibrillation, Heart Failure with Preserved Ejection Fraction (HFpEF), Familial Progressive Cardiac Conduction Defect, and Pancreaticoduodenectomy.

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    Last Updated: 06/30/2026

    What is the definition of Isovaleric Acidemia?

    Isovaleric acidemia (IVA) occurs when the body cannot breakdown certain parts of the proteins found in food. This can cause a build-up of toxic substances which can lead to bouts of serious illness known as metabolic crises. There are two types of IVA. The acute, neonatal type has more severe symptoms. In the chronic, intermittent type symptoms can come and go. Symptoms include poor feeding, tremor, vomiting, low muscle tone, and lack of energy (lethargy). One characteristic sign of IVA is an odor of sweaty feet during illness. IVA occurs due to variants in the IVD gene and is inherited in an autosomal recessive pattern. Diagnosis of IVD is based on the symptoms, clinical exam, and blood and urine testing. The results of genetic testing may help confirm the diagnosis.
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