The 20 Best Abruzzo-Erickson Syndrome Doctors Near Me in rancho cucamonga, CA

Find the Top Abruzzo-Erickson Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Abruzzo-Erickson Syndrome near rancho cucamonga, CA. Of these, 2 are Experienced.

Location
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2 providers found
    Experienced in Abruzzo-Erickson Syndrome
    Family Medicine
    Experienced in Abruzzo-Erickson Syndrome
    Family Medicine

    9190 Haven Ave

    9190 Haven Ave Ste 102, 
    Rancho Cucamonga, CA 
     (0.9 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Ani Berberyan is a primary care provider, practicing in Family Medicine in Rancho Cucamonga, California. Dr. Berberyan is rated as an Experienced provider by MediFind in the treatment of Abruzzo-Erickson Syndrome. She is also highly rated in 11 other conditions, according to our data. Her clinical expertise encompasses Obesity, Axillary Nerve Dysfunction, Sciatica, and High Cholesterol. Dr. Berberyan is currently accepting new patients.

    Experienced in Abruzzo-Erickson Syndrome
    Medical Genetics | Pediatrics
    Experienced in Abruzzo-Erickson Syndrome
    Medical Genetics | Pediatrics
    Referral may be required

    Faculty Physicians And Surgeons Of Llusm

    901 San Bernardino Rd, Suite 104and302, 
    Upland, CA 
     (2.6 miles away)
    Languages Spoken:
    English

    Hua Wang is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Upland, California. Dr. Wang is rated as an Experienced provider by MediFind in the treatment of Abruzzo-Erickson Syndrome. Her clinical expertise encompasses Miller-Dieker Syndrome, Smith-Magenis Syndrome, Hypochondroplasia, and Achondroplasia.

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    Last Updated: 09/26/2026

    What is the definition of Abruzzo-Erickson Syndrome?

    Abruzzo-Erickson syndrome is an extremely rare condition characterized by cleft palate, coloboma, hypospadius, deafness, short stature, and radioulnar synostosis. Although the underlying cause of the condition is still being studied, it appears to result, at least in part, from genetic changes in the TBX22 gene. The condition is inherited in an X-linked recessive manner.

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