The 20 Best Chromosome 13q Deletion Doctors Near Me in san francisco, CA

Find the Top Chromosome 13q Deletion Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 1 doctor with experience in Chromosome 13q Deletion near san francisco, CA. Of these, 1 are Experienced.

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1 provider found
    Experienced in Chromosome 13q Deletion
    Medical Genetics
    Experienced in Chromosome 13q Deletion
    Medical Genetics
    Referral may be required

    Adult Neurofibromatosis Type 1 (NF1) And Schwannomatosis Clinic

    400 Parnassus Ave., Eighth Floor, 
    San Francisco, CA 
     (2.2 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Joseph Shieh is a Medical Genetics provider practicing medicine in San Francisco, California. Dr. Shieh is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Deletion. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Neurofibromatosis Type 1 (NF1), Myhre Syndrome, Ectodermal Dysplasias, and Clouston Syndrome. Dr. Shieh is board certified in American Board Of Medical Genetics And Genomics, Clinical Genetics And Genomics. Dr. Shieh is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Chromosome 13q Deletion?

    Chromosome 13q deletion is a chromosome abnormality that occurs when there is a missing (deleted) copy of genetic material on the long arm (q) of chromosome 13. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with Chromosome 13q deletion include developmental delay, intellectual disability, behavioral problems and distinctive facial features. Chromosome testing of both parents can provide more information on whether or not the deletion was inherited. In most cases, parents do not have any chromosomal anomaly. However, sometimes one parent is found to have a balanced translocation, where a piece of a chromosome has broken off and attached to another one with no gain or loss of genetic material. The balanced translocation normally does not cause any signs or symptoms, but it increases the risk for having an affected child with a chromosomal anomaly like a deletion.

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