The 20 Best Dubowitz Syndrome Doctors Near Me in warren, OH

Find the Top Dubowitz Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Dubowitz Syndrome near warren, OH. Of these, 2 are Experienced.

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2 providers found
    Experienced in Dubowitz Syndrome
    Experienced in Dubowitz Syndrome
    Referral may be required

    Trumbull Regional Medical Center

    1350 E Market St, 
    Warren, OH 
     (1.0 miles away)
    330-841-9011
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients

    Rany Aburashed is a Neurologist practicing medicine in Warren, Ohio. Dr. Aburashed is rated as an Experienced provider by MediFind in the treatment of Dubowitz Syndrome. He is also highly rated in 15 other conditions, according to our data. His clinical expertise encompasses Multiple Sclerosis (MS), Relapsing Multiple Sclerosis (RMS), Epilepsy, and Seizures. Dr. Aburashed is currently accepting new patients.

    Experienced in Dubowitz Syndrome

    Dr. Tolga Icli
    Family Medicine
    Experienced in Dubowitz Syndrome

    Dr. Tolga Icli
    Family Medicine

    Medical Outpatient Center - B, Atintown

    1450 South Canfield Niles Road, Suite A, 
    Atintown, OH 
     (9.8 miles away)
    234-264-8333
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients

    Tolga Icli is a primary care provider, practicing in Family Medicine in Atintown, Ohio. Dr. Icli is rated as an Experienced provider by MediFind in the treatment of Dubowitz Syndrome. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Homocystinuria, Methylmalonic Acidemia with Homocystinuria, Inborn Amino Acid Metabolism Disorder, and Familial Hypertriglyceridemia. Dr. Icli is board certified in American Board Of Family Medicine, 2014. Dr. Icli is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Dubowitz Syndrome?

    Dubowitz syndrome is a very rare genetic and developmental disorder with a broad range of signs and symptoms. The typical findings of Dubowitz syndrome include growth failure/short stature, characteristic facial features such as a small triangular face, high sloping forehead, drooping eyelid (ptosis), short eyelids, increased distance between eyes (hypertelorism) broad and flat nasal bridge with a prominent and rounded nasal tip, smaller than normal head (microcephaly), intellectual disability, and eczema, especially on the face and behind the knees. Other common findings are behavioral disorders (hyperactivity, and/or autistic features), speech alterations, scanty or absent hair, foot abnormalities, delayed bone age, bone defects of the lower part of the spine (sacrum and coccyx), testicles that are still not located in the scrotum (cryptorchidism), memory and / or learning problems. There may be an increased risk of having cancer such as leukemia, or lymphoma. The diagnosis is made based on the symptoms (specially the facial features), but there is no specific laboratory test. The cause is still unknown, but, some people who are diagnosed with the syndrome may have variants in the NSUN2 and LIG4 genes, or have loss or gain of microscopic material in some chromosomes (chromosomal microdeletions or microduplications).