The 20 Best Dubowitz Syndrome Doctors Near Me in syracuse, NY

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 syracuse, NY. Of these, 2 are Experienced.

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2 providers found
    Experienced in Dubowitz Syndrome
    Internal Medicine
    Experienced in Dubowitz Syndrome
    Internal Medicine

    Upstate Specialty Services At Harrison Center-Hepatobiliary And Pancreatic Surgery Program

    550 Harrison St Ste I, 
    Syracuse, NY 
     (0.4 miles away)
    Languages Spoken:
    English
    Offers Telehealth

    Sarah Lappin is a primary care provider, practicing in Internal Medicine in Syracuse, New York. Dr. Lappin is rated as an Experienced provider by MediFind in the treatment of Dubowitz Syndrome. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Familial Hypertension, Hypertension, Glucocorticoid-Remediable Aldosteronism, and Sitosterolemia.

    Experienced in Dubowitz Syndrome
    Internal Medicine
    Experienced in Dubowitz Syndrome
    Internal Medicine

    Upstate Health Care Center-Dermatology Outpatient Clinic

    90 Presidential Plz Fl 2, 
    Syracuse, NY 
     (0.4 miles away)
    Languages Spoken:
    English

    Caitlin Toomey is a primary care provider, practicing in Internal Medicine in Syracuse, New York. Dr. Toomey is rated as an Experienced provider by MediFind in the treatment of Dubowitz Syndrome. Her clinical expertise encompasses Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Langer Mesomelic Dysplasia, and Pena-Shokeir Syndrome Type 2.

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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).
    15 miles has been selected.