[P1-12] Poster Session 1-12　Pediatric Genetics 1

[P1-12-16] A case of ACTA2 mutation with various symptoms from the fetal period

^○Ayana Tsuboi^1,2, Hisako Saiki³, Satoshi Hirahara⁴, Naomi Kamei⁴, Kazuhiro Ohtsu⁴, Hanae Satano¹, Rie Fukuhara³, Mihoko Doi¹, Toshiki Takenouchi⁵, Kenjiro Kosaki⁶ (1.Department of Genomic Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan, 2.Department of Pediatrics, Hiroshima Prefectural Hospital, Hiroshima, Japan, 3.Department of Neonatology, Hiroshima Prefectural Hospital, Hiroshima, Japan, 4.Department of Pediatrics Surgery, Hiroshima Prefectural Hospital, Hiroshima, Japan, 5.Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan, 6.Center of MedicalGenetics, Keio University School of medicine, Tokyo, Japan)

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