The 20 Best Dubowitz Syndrome Doctors Near Me in pocatello, ID

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 pocatello, ID. Of these, 2 are Experienced.

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2 providers found
    Experienced in Dubowitz Syndrome

    Dr. Jon D. Malan
    Family Medicine
    Experienced in Dubowitz Syndrome

    Dr. Jon D. Malan
    Family Medicine
    Before you request

    Health West City Center

    1001 N 7th Ave, 
    Pocatello, ID 
     (0.9 miles away)
    208-425-2489
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients
    Offers Telehealth

    Jon Malan is a primary care provider, practicing in Family Medicine in Pocatello, Idaho. Dr. Malan is rated as an Experienced provider by MediFind in the treatment of Dubowitz Syndrome. He is also highly rated in 6 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Chronic Obstructive Pulmonary Disease (COPD), and Hypertension. Dr. Malan is board certified in American Board Of Family Medicine. Dr. Malan is currently accepting new patients.

    Experienced in Dubowitz Syndrome
    Experienced in Dubowitz Syndrome

    Portneuf Primary Care At Northgate

    2850 Olympus Dr, 
    Pocatello, ID 
     (4.6 miles away)
    208-239-3815
    Languages Spoken:
    English, Spanish
    See accepted insurances
    Accepting New Patients

    Yolanda Rodriguez-Valdivia is a primary care provider, practicing in Family Medicine in Pocatello, Idaho. Dr. Rodriguez-Valdivia is rated as an Experienced provider by MediFind in the treatment of Dubowitz Syndrome. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Hypothyroidism, Obesity in Children, Type 2 Diabetes (T2D), and Nephrosclerosis. Dr. Rodriguez-Valdivia 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).