The 20 Best Congenital Radioulnar Synostosis Doctors Near Me in seattle, WA

Find the Top Congenital Radioulnar Synostosis Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 3 doctor with experience in Congenital Radioulnar Synostosis near seattle, WA. Of these, 2 are Experienced and 1 are Advanced.

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3 providers found
    Experienced in Congenital Radioulnar Synostosis
    Orthopedics | Hand Surgery
    Experienced in Congenital Radioulnar Synostosis
    Orthopedics | Hand Surgery
    Referral may be required

    Proliance Surgeons

    5350 Tallman Ave NW, Ste 500, 
    Seattle, WA 
     (4.7 miles away)
    Languages Spoken:
    English, Hindi, Korean, Mandarin, Spanish
    Accepting New Patients
    Offers Telehealth

    Wayne Weil is an Orthopedics specialist and a Hand Surgeon practicing medicine in Seattle, Washington. Dr. Weil is rated as an Experienced provider by MediFind in the treatment of Congenital Radioulnar Synostosis. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Dupuytren Contracture, Rhizarthrosis, Carpal Tunnel Syndrome, Ganglion Cyst, and Hip Replacement. Dr. Weil is board certified in American Board Of Orthopaedic Surgery. Dr. Weil is currently accepting new patients.

    Advanced in Congenital Radioulnar Synostosis
    Advanced in Congenital Radioulnar Synostosis
    Referral may be required

    Seattle Children's Hospital

    4800 Sand Point Way NE, 
    Seattle, WA 
     (4.5 miles away)
    Languages Spoken:
    English, Danish, French, Spanish
    Accepting New Patients
    Offers Telehealth

    Suzanne Steinman is an Orthopedics provider practicing medicine in Seattle, Washington. Dr. Steinman is rated as an Advanced provider by MediFind in the treatment of Congenital Radioulnar Synostosis. She is also highly rated in 17 other conditions, according to our data. Her clinical expertise encompasses Hereditary Multiple Osteochondromas, Preaxial Polydactyly Type 1, Congenital Radioulnar Synostosis, Sprengel Deformity, and Osteotomy. Dr. Steinman is currently accepting new patients.

    Experienced in Congenital Radioulnar Synostosis
    Family Medicine
    Experienced in Congenital Radioulnar Synostosis
    Family Medicine

    Highlands Clinic - Primary Care

    3901 NE 4th St, Ste 105, 
    Renton, WA 
     (11.3 miles away)
    Languages Spoken:
    English, Arabic
    Accepting New Patients
    Offers Telehealth

    Mariel Scheinberg is a primary care provider, practicing in Family Medicine in Renton, Washington. Dr. Scheinberg is rated as an Experienced provider by MediFind in the treatment of Congenital Radioulnar Synostosis. Her clinical expertise encompasses Obesity, Obesity in Children, Hypertension, and Glucocorticoid-Remediable Aldosteronism. Dr. Scheinberg is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Congenital Radioulnar Synostosis?

    Congenital radioulnar synostosis is a rare condition in which there is an abnormal connection (synostosis) of the radius and ulna (bones in the forearm) at birth. The condition is present in both arms (bilateral) in approximately 60% of cases. Signs and symptoms depend on the severity of the abnormality and whether it is bilateral; people with the condition often have limited rotational movement of the forearm. Pain is usually not present until the teenage years. There are 2 types of radioulnar synostosis: type 1 and type 2. In type 1, the fusion involves 2-6 cm of the area between the radius and ulna bones which is closer to the elbow and the knobby end of the radius that meets the elbow is absent (radial head). In type 2, the fusion is farther from the elbow and there is dislocation of the radial head. Both types result in a limitation of inward roll (pronation) and outward roll (supination) of the forearm, and in type 2 there is also a restriction of extension at the elbow. Congenital radioulnar synostosis is due to abnormal fetal development of the forearm bones, but the underlying cause is not always known. It is sometimes a feature of certain chromosome abnormalities or genetic syndromes. Some cases appear to be inherited in an autosomal dominant manner.