Department of Surgery, Division of Pediatrics Saint Louis University School of Medicine, Saint Louis, Missouri.
Department of Pediatrics, Division of Medical Genetics, Saint Louis University School of Medicine, Saint Louis, Missouri.
Am J Med Genet A. 2019 May;179(5):817-821. doi: 10.1002/ajmg.a.61078. Epub 2019 Feb 20.
Retinoic acid receptor beta (RARB) variants are heavily linked to pathologies of neural crest cell migration. The purpose of this report is to present a 23-month-old male with the previously described R387C RARB gain-of-function variant whose gastrointestinal issues and long-term constipation lead to the discovery of colonic hypoganglionosis. This case further delineates the pattern of malformation associated with RARB variants. The findings are also consistent with the known etiology of aganglionic colon due to failed neural crest cell migration.
视黄酸受体β(RARB)变体与神经嵴细胞迁移的病理学密切相关。本报告的目的是介绍一例 23 个月大的男性,其携带先前描述的 RARB 获得性功能变体 R387C,该变体导致胃肠道问题和长期便秘,进而发现结肠低神经节细胞症。该病例进一步阐明了与 RARB 变体相关的畸形模式。这些发现也与已知的由于神经嵴细胞迁移失败导致无神经节结肠的病因一致。