The 20 Best Acrocephalopolydactyly Doctors in New Zealand

Find the Top Acrocephalopolydactyly Experts and Specialists

Last Updated: 06/30/2026

Save doctors for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Already have a doctor?
Find A Second Opinion

MediFind found 2 doctor with experience in Acrocephalopolydactyly near New Zealand. Of these, 2 are Experienced.

Location
LocationClose
2 providers found
    Experienced in Acrocephalopolydactyly
    Experienced in Acrocephalopolydactyly
    Referral may be required
    Dunedin, OTA, NZ 

    Peter Fowler practices practicing medicine in Dunedin, New Zealand. Mr. Fowler is rated as an Experienced expert by MediFind in the treatment of Acrocephalopolydactyly. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Cleft Lip and Palate, Apert Syndrome, Acrocephalopolydactyly, Osteotomy, and Bone Graft.

    Experienced in Acrocephalopolydactyly
    Experienced in Acrocephalopolydactyly
    Referral may be required
    2 Park Road, 
    Grafton, AUK, NZ 

    Jeyasakthy Saniasiaya practices practicing medicine in Grafton, New Zealand. Saniasiaya is rated as an Experienced expert by MediFind in the treatment of Acrocephalopolydactyly. They are also highly rated in 11 other conditions, according to our data. Their clinical expertise encompasses Vertigo, Otitis, Otitis Media with Effusion, Myringotomy, and Endoscopy.

    Learn about our expert tiers
    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
    Showing 1-2 of 2

    Last Updated: 06/30/2026

    What is the definition of Acrocephalopolydactyly?

    Acrocephalopolydactyly, also known as Elejalde syndrome, is an extremely rare genetic (autosomal recessive) disorder characterized by excessive birth weight and facial, body, organ, limb, and finger abnormalities. Fewer than twelve cases have been identified.
    Recommended has been selected.