The 20 Best Mosaic Trisomy 9 Doctors Near Me in Eskisehir, 26

Find the Top Mosaic Trisomy 9 Experts and Specialists

Last Updated: 04/28/2026

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MediFind found 6 doctor with experience in Mosaic Trisomy 9 near Eskisehir, 26. Of these, 6 are Experienced.

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6 providers found
    Experienced in Mosaic Trisomy 9
    Experienced in Mosaic Trisomy 9
    Eskisehir, TR 
     (1.8 km away)

    Sevilhan Artan practices practicing medicine in Eskisehir, Turkey. Artan is rated as an Experienced expert by MediFind in the treatment of Mosaic Trisomy 9. They are also highly rated in 3 other conditions, according to our data. Their clinical expertise encompasses Chromosome 5q Duplication, Hydranencephaly, Chromosome 22 Duplication, and Microcephaly with Spastic Quadriplegia.

    Experienced in Mosaic Trisomy 9
    Experienced in Mosaic Trisomy 9
    Eskisehir, TR 
     (1.8 km away)

    Ebru Gokalp practices practicing medicine in Eskisehir, Turkey. Ms. Gokalp is rated as an Experienced expert by MediFind in the treatment of Mosaic Trisomy 9. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Chromosome 5q Duplication, Hydranencephaly, Chromosome 22 Duplication, and Microcephaly with Spastic Quadriplegia.

    Experienced in Mosaic Trisomy 9
    Experienced in Mosaic Trisomy 9
    Eskisehir, TR 
     (1.8 km away)

    Sinem Kocagil practices practicing medicine in Eskisehir, Turkey. Ms. Kocagil is rated as an Experienced expert by MediFind in the treatment of Mosaic Trisomy 9. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Chromosome 5q Duplication, Hydranencephaly, Chromosome 22 Duplication, and Microcephaly with Spastic Quadriplegia.

    Learn about our expert tiers
    Experienced in Mosaic Trisomy 9
    Experienced in Mosaic Trisomy 9
    Eskisehir, TR 
     (1.8 km away)

    Ozcan Bor practices practicing medicine in Eskisehir, Turkey. Bor is rated as an Experienced expert by MediFind in the treatment of Mosaic Trisomy 9. They are also highly rated in 11 other conditions, according to our data. Their clinical expertise encompasses Childhood Iron Deficiency Anemia, Chromosome 5q Duplication, Infantile Neutropenia, Febrile Neutropenia, and Bone Marrow Aspiration.

    Experienced in Mosaic Trisomy 9
    Experienced in Mosaic Trisomy 9
    Eskisehir, TR 
     (1.8 km away)

    Oguz Cilingir practices practicing medicine in Eskisehir, Turkey. Mr. Cilingir is rated as an Experienced expert by MediFind in the treatment of Mosaic Trisomy 9. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Chromosome 5q Duplication, Hydranencephaly, Chromosome 22 Duplication, and Deafness Hypogonadism Syndrome.

    Experienced in Mosaic Trisomy 9
    Experienced in Mosaic Trisomy 9
    Eskisehir, TR 
     (1.8 km away)

    Beyhan Aras practices practicing medicine in Eskisehir, Turkey. Aras is rated as an Experienced expert by MediFind in the treatment of Mosaic Trisomy 9. They are also highly rated in 3 other conditions, according to our data. Their clinical expertise encompasses Chromosome 5q Duplication, Hydranencephaly, Chromosome 22 Duplication, and Microcephaly with Spastic Quadriplegia.

    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 1-6 of 6

    Last Updated: 04/28/2026

    What is the definition of Mosaic Trisomy 9?

    Mosaic trisomy 9 is a chromosomal abnormality that can affect may parts of the body. In people affected by this condition, some of the body's cells have three copies of chromosome 9 (trisomy), while other cells have the usual two copies of this chromosome. The signs and symptoms vary but may include mild to severe intellectual disability, developmental delay, growth problems (both before and after birth), congenital heart defects, and/or abnormalities of the craniofacial (skull and face) region. Most cases are not inherited; it often occurs sporadically as a random event during the formation of the reproductive cells (egg and sperm) or as the fertilized egg divides.
    15 km has been selected.