The 20 Best Dubowitz Syndrome Doctors Near Me in mitchell, SD

Find the Top Dubowitz Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 1 doctor with experience in Dubowitz Syndrome near mitchell, SD. Of these, 1 are Advanced.

Location
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1 provider found
    Advanced in Dubowitz Syndrome
    Internal Medicine
    Advanced in Dubowitz Syndrome
    Internal Medicine

    Access Health & Avera Medical Group Family Health Center — Mitchell

    1900 Grassland Dr, Suite 103, 
    Mitchell, SD 
     (1.4 miles away)
    Languages Spoken:
    English, Filipino
    Accepting New Patients

    Jonathan Olegario is a primary care provider, practicing in Internal Medicine in Mitchell, South Dakota. Dr. Olegario is rated as an Advanced provider by MediFind in the treatment of Dubowitz Syndrome. He is also highly rated in 51 other conditions, according to our data. His clinical expertise encompasses High Cholesterol, Sitosterolemia, Renovascular Hypertension, and Chronic Cough. Dr. Olegario is board certified in American Board Of Internal Medicine. Dr. Olegario 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).