The 59th Annual Meeting of the Japanese Society of Child Neurology

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Oral Presentation

genetic abnormality

[O17] Oral Presentation
teratology 3 -case report-

Fri. Jun 16, 2017 4:20 PM - 5:30 PM Room No.6 (10F Conference Room 1009)

Chair:Shinji Saitoh(Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan), Shinsuke Ninomiya(Department of Clinical Genetics, Kurashiki Central Hospital, Okayama, Japan)

[O-097] Joubert syndrome and related disorders with congenital oculomotor apraxia and NPHP1 gene deletion

○Nahoko Katayama1, Ryosuke Urabe1, Tetsuharu Kamioka1, Yu Kakimoto1, Go Takei1, Hiroshi Terashima1, Masaya Kubota1, Rika Kosaki2, Akira Oka3 (1.Division of Neurology, National Center for Child Health and Development, Tokyo, Japan, 2.Division of Medical Genetics. National Center for Child Health and Development, Tokyo, Japan, 3.Department of Pediatrics, The University of Tokyo Hospital, Tokyo, Japan)

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