The 20 Best Spondylocarpotarsal Synostosis Syndrome Doctors Near Me in modesto, CA

Find the Top Spondylocarpotarsal Synostosis Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Spondylocarpotarsal Synostosis Syndrome near modesto, CA. Of these, 2 are Experienced.

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2 providers found
    Experienced in Spondylocarpotarsal Synostosis Syndrome
    Family Medicine
    Experienced in Spondylocarpotarsal Synostosis Syndrome
    Family Medicine

    Golden Valley Health Center

    1920 Memorial Dr, 
    Ceres, CA 
     (3.4 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Daniel Diep is a primary care provider, practicing in Family Medicine in Ceres, California. Dr. Diep is rated as an Experienced provider by MediFind in the treatment of Spondylocarpotarsal Synostosis Syndrome. He is also highly rated in 112 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Familial Hypertension, Glucocorticoid-Remediable Aldosteronism, Hypertension, and Intrauterine Device Insertion. Dr. Diep is currently accepting new patients.

    Experienced in Spondylocarpotarsal Synostosis Syndrome
    Experienced in Spondylocarpotarsal Synostosis Syndrome
    Referral may be required

    Modesto Advanced Diagnostic Imaging Medical Center

    157 E Coolidge Ave, 
    Modesto, CA 
     (1.9 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Douglas Tait is a Radiologist practicing medicine in Modesto, California. Dr. Tait is rated as an Experienced provider by MediFind in the treatment of Spondylocarpotarsal Synostosis Syndrome. He is also highly rated in 27 other conditions, according to our data. His clinical expertise encompasses Tenosynovitis, Breast Lump, Scoliosis, and Nabothian Cyst. Dr. Tait is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Spondylocarpotarsal Synostosis Syndrome?

    Spondylocarpotarsal synostosis (SCT) syndrome is an inherited syndrome characterized by disproportionate short stature, abnormalities of the vertebrae in the spine, scoliosis and lordosis, carpal and tarsal fusion (fusion of the bones in the hands and feet), clubfoot, and facial abnormalities such as round face, large forehead, and up-turned nostrils. Other features can include cleft palate, deafness, loose joints, and poor formation of tooth enamel. SCT syndrome has been associated with retinal anomalies and cataracts. However, these eye problems are usually not severe enough to impair vision. This condition is caused by genetic changes in the FLNB gene. It is inherited in an autosomal recessive manner in families, which means that parents are usually unaffected and children have to have inherited a genetic change from each parent.