[S2] Symposium 2　Genetic Practice in Mitochondrial Disease  | The 69th Annual Meeting of the Japan Society of Human Genetics

Session Details

Symposium

[S2]Symposium 2　Genetic Practice in Mitochondrial Disease

Thu. Oct 10, 2024 8:30 AM - 10:30 AM JST
Thu. Oct 10, 2024 11:30 PM - 1:30 AM UTC

Room 2（Ballroom A, 3F）

Chairs：Kei Murayama（Diagnostics and Therapeutics of Intractable Disease, Intractable Disease Research Center. Department of Pediatrics, Juntendo University Faculty of Medicine）, Masakazu Mimaki（Department of Pediatrics, Teikyo University School of Medicine）

[S2_video]【Video】Symposium 2 Genetic Practice in Mitochondrial Disease

[S2-1]General Topics of Mitochondrial Diseases

^○Yuichi Goto^1,2 (1.Medical Genome Center, National Center of Neurology and Psychiatry, 2.National Center Biobank Network, National Center for Global Health and Medicine)

[S2-2]Comprehensive Mitochondrial Disease Gene Panel Sequencing

^○Yasushi Okazaki^1,2, Kei Murayama¹ (1.Juntendo University, Tokyo, Japan, 2.IMS RIKEN, Yokohama, Japan)

[S2-3]Genetic medicine for mitochondrial hearing loss

^○Tatsuo Matsunaga^1,2,3 (1.Division of Hearing and Balance Research, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan, 2.Medical Genetics Center, National Hospital Organization Tokyo Medical Center, Tokyo, Japan, 3.Department of Otolaryngology, National Hospital Organization Tokyo Medical Center, Tokyo, Japan)

[S2-4]Early diagnosis and accurate treatment of mitochondrial nephropathy

^○Toshiyuki Imasawa (Department of Nephrology, National Hospital Organization Chiba-Higashi National Hospital)

[S2-5]Current Status of Prenatal and Preimplantation Diagnosis for Mitochondrial Diseases

^○Akira Namba (Department of Clinical Genomics, Saitama Medical University Hospital)

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Session Details