The 20 Best Homocystinuria due to MTHFR Deficiency Doctors Near Me in Uttar Pradesh, IN

Find the Top Homocystinuria due to MTHFR Deficiency Experts and Specialists

Last Updated: 06/30/2026

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MediFind found 6 doctor with experience in Homocystinuria due to MTHFR Deficiency near Uttar Pradesh, IN. Of these, 6 are Experienced.

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6 providers found
    Experienced in Homocystinuria due to MTHFR Deficiency
    Experienced in Homocystinuria due to MTHFR Deficiency
    Referral may be required
    Raebareli Road, 
    Lucknow, UP, IN 

    Amita Moirangthem practices practicing medicine in Lucknow, India. Ms. Moirangthem is rated as an Experienced expert by MediFind in the treatment of Homocystinuria due to MTHFR Deficiency. She is also highly rated in 13 other conditions, according to our data. Her clinical expertise encompasses Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia, Camptodactyly Taurinuria, Camptodactyly Syndrome Guadalajara Type 1, and Camptodactyly Syndrome Guadalajara Type 2.

    Experienced in Homocystinuria due to MTHFR Deficiency
    Experienced in Homocystinuria due to MTHFR Deficiency
    Referral may be required
    Raebareli Road, 
    Lucknow, UP, IN 

    Arya Shambhavi practices practicing medicine in Lucknow, India. Shambhavi is rated as an Experienced expert by MediFind in the treatment of Homocystinuria due to MTHFR Deficiency. They are also highly rated in 1 other condition, according to our data. Their clinical expertise encompasses Hereditary Spastic Paraparesis, Spastic Paraparesis, Homocystinuria due to MTHFR Deficiency, and Spasticity.

    Experienced in Homocystinuria due to MTHFR Deficiency
    Experienced in Homocystinuria due to MTHFR Deficiency
    Referral may be required
    Raebareli Road, 
    Lucknow, UP, IN 

    Shubha Phadke practices practicing medicine in Lucknow, India. Ms. Phadke is rated as an Experienced expert by MediFind in the treatment of Homocystinuria due to MTHFR Deficiency. She is also highly rated in 38 other conditions, according to our data. Her clinical expertise encompasses Camptodactyly Taurinuria, Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia, Camptodactyly Syndrome Guadalajara Type 1, and Camptodactyly Syndrome Guadalajara Type 2.

    Learn about our expert tiers
    Experienced in Homocystinuria due to MTHFR Deficiency
    Experienced in Homocystinuria due to MTHFR Deficiency
    Referral may be required
    UP, IN 

    Suzena Masih practices practicing medicine in India. Masih is rated as an Experienced expert by MediFind in the treatment of Homocystinuria due to MTHFR Deficiency. They are also highly rated in 6 other conditions, according to our data. Their clinical expertise encompasses Achalasia Microcephaly Syndrome, Microcephaly, Renpenning Syndrome, and Rhizomelic Syndrome.

    Experienced in Homocystinuria due to MTHFR Deficiency
    Experienced in Homocystinuria due to MTHFR Deficiency
    Referral may be required
    Raebareli Road, 
    Lucknow, UP, IN 

    Deepti Saxena practices practicing medicine in Lucknow, India. Ms. Saxena is rated as an Experienced expert by MediFind in the treatment of Homocystinuria due to MTHFR Deficiency. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Pycnodysostosis, Congenital Contractures, Arthrogryposis Multiplex Congenita, and Fetal Akinesia Sequence.

    Experienced in Homocystinuria due to MTHFR Deficiency
    Experienced in Homocystinuria due to MTHFR Deficiency
    Referral may be required
    Raebareli Road, 
    Lucknow, UP, IN 

    Mayank Nilay practices practicing medicine in Lucknow, India. Mr. Nilay is rated as an Experienced expert by MediFind in the treatment of Homocystinuria due to MTHFR Deficiency. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Rhizomelic Syndrome, Genital Dwarfism, and Robinow Syndrome.

    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
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    Last Updated: 06/30/2026

    What is the definition of Homocystinuria due to MTHFR Deficiency?

    Homocystinuria due to MTHFR deficiency is a genetic condition that results from poor metabolism of folate (also called vitamin B9), due to a lack of working enzyme called MTHFR. The gene that tells our body how to make the enzyme is also called MTHFR. At least 40 rare MTHFR gene variants have been found in people with decreased or no working enzyme. Very common gene variants (C677T and A1298C) can cause some decrease in enzyme function. People with Homocystinuria due to MTHFR deficiency tend to have two rare variants or sometimes a rare variant and a common variant. Very rarely people inherit a combination of three or four common variants from their parents (for example two C677T variants and two A1298C variants) and may also develop very high levels of homocystine in their body. Homocystinuria usually does not show symptoms in a newborn baby. Symptoms may include abnormal clotting, developmental delay, seizures, intellectual disability, and microcephaly. Severe homocystinuria can also be caused by gene variants in other genes besides MTHFR.