Asakura Yuta, Osaka Hitoshi, Aoi Hiromi, Mizuguchi Takeshi, Matsumoto Naomichi, Yamagata Takanori
Department of Pediatrics, Jichi Medical University, Tochigi, Japan.
Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Hum Genome Var. 2021 Aug 17;8(1):34. doi: 10.1038/s41439-021-00165-7.
Mutations in a number of genes related to chromosomal segregation reportedly cause developmental disorders, e.g., chromosome alignment-maintaining phosphoprotein 1 (CHAMP1). We report on an 8-year-old Japanese girl who presented with a developmental disorder and microcephaly and carries a novel nonsense mutation in CHAMP1. Therefore, CHAMP1 mutation should be considered as a differential diagnosis of global developmental delay and microcephaly.
据报道,一些与染色体分离相关的基因突变会导致发育障碍,例如染色体排列维持磷蛋白1(CHAMP1)。我们报告了一名8岁的日本女孩,她患有发育障碍和小头畸形,并且在CHAMP1基因中携带一种新的无义突变。因此,CHAMP1突变应被视为全球发育迟缓与小头畸形的鉴别诊断因素。