The 20 Best Chromosome 9p Deletion Doctors in Hong Kong

Find the Top Chromosome 9p Deletion Experts and Specialists

Last Updated: 06/30/2026

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MediFind found 2 doctor with experience in Chromosome 9p Deletion near Hong Kong. Of these, 2 are Advanced.

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2 providers found
    Advanced in Chromosome 9p Deletion
    Advanced in Chromosome 9p Deletion
    Referral may be required
    19, Eastern Hospital Road, 
    Causeway Bay, HEA, HK 

    Ching Leung practices practicing medicine in Causeway Bay, Hong Kong Special Administrative Region. Leung is rated as an Advanced expert by MediFind in the treatment of Chromosome 9p Deletion. They are also highly rated in 3 other conditions, according to our data. Their clinical expertise encompasses Chromosome 9p Deletion, Freeman-Sheldon Syndrome, Neurofibromatosis Type 2 (NF2), and Neurofibromatosis.

    Advanced in Chromosome 9p Deletion
    Advanced in Chromosome 9p Deletion
    Referral may be required
    19, Eastern Hospital Road, 
    Causeway Bay, HEA, HK 

    Chuen Ko practices practicing medicine in Causeway Bay, Hong Kong Special Administrative Region. Ko is rated as an Advanced expert by MediFind in the treatment of Chromosome 9p Deletion. They are also highly rated in 1 other condition, according to our data. Their clinical expertise encompasses Chromosome 9p Deletion, Freeman-Sheldon Syndrome, Neurofibromatosis Type 2 (NF2), and Anophthalmia Plus Syndrome.

    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.
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    Last Updated: 06/30/2026

    What is the definition of Chromosome 9p Deletion?

    Chromosome 9p deletion is a chromosome abnormality that occurs when there is a missing (deleted) copy of genetic material on the short arm (p) of chromosome 9. The severity and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features may affect many parts of the body and may include developmental delay, low muscle tone (hypotonia), distinctive facial features, heart conditions, scoliosis, and/or genital abnormalities. Chromosome testing of both parents can provide more information on whether the deletion was inherited. In about half of cases, the deletion occurs sporadically and neither parent has a chromosome abnormality. In the other half, one parent is found to have the same deletion (possibly with no features) or a balanced translocation (which usually does not cause any features).