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发育医学电子杂志  2026, Vol. 14 Issue (3): 261-265    DOI: xushan68@163.com
  生长发育   病例报告 |
DDX3X 基因变异致DDX3X相关神经发育障碍并发中枢性性早熟 1 例报道
张淑颖 连群 李伶俐 曾会勤 宋佳 许珊珊
厦门大学附属第一医院 儿科  厦门大学医学院,福建 厦门 361003
A case report of DDX3X-related neurodevelopmental disorder caused by DDX3X variant complicated with central precocious puberty
Zhang Shuying, Lian Qun, Li Lingli, et al.
Department of Pediatrics, the First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian 361003, China
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摘要 
DDX3X 相 关 神 经 发 育 障 碍(DDX3X-related neurodevelopmental disorder,DDX3X-NDD ;OMIM :300958)是一种X连锁的神经发育障碍性疾病,可累及多系统,目前国内尚无由 DDX3X 基因变异所致的性早熟病例报道。本文报道1例 2019年初次就诊于厦门大学附属第一医院,由 DDX3X 基因新发剪切变异(c.1171-1G>A)所致 DDX3X-NDD 并发中枢性性早熟(central precocious puberty, CPP)女性患儿。系 8 岁 5 个月女性,因乳房发育半年、阴毛出现 2 个月就诊,伴有注意缺陷与多动障碍、精神发育迟缓表现,完善实验室检查符合 CPP,全外显子组测序发现患者 DDX3X 基因杂合变异(c.1171-1G>A),父母均为野生型。应用促性腺激素释放激素类似物治疗 17 个月,效果良好。本文通过总结该例由 DDX3X 基因变异所致 DDX3X-NDD 并发 CPP 患者的临床表现,以提高临床医师对该 2 种疾病的认识。
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Abstract: 
DDX3X-related neurodevelopmental disorder (DDX3X-NDD) is an X-linked neurodevelopmental disorder that can affect multiple systems. This is the first report of precocious puberty caused by DDX3X genetic variants in China at present. This article reports a patient with DDX3X-NDD complicated with central precocious puberty (CPP), caused by a novel DDX3X gene splicing variant (c.1171-1G>A), who was initially treated at the First Affiliated Hospital of Xiamen University in 2019. She was an 8-year-5-month old girl came to clinic because of breast development and pubic hair appearance, accompanied by attention deficit and hyperactive disorder and mental retardation. Laboratory tests were consistent with CPP puberty. Whole exome sequencing revealed a de novo heterozygous variant in DDX3X gene (c.1171-1G>A, her parents were wild-type). Then the patient received 17 months gonadotropin-releasing hormone analogue (GnRHa) treatment, and reflects well. By summarizing the clinical manifestations of DDX3X-NDD complicated with CPP caused by DDX3X variant, aims to enhance clinicians' understanding of these two diseases.
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收稿日期:  2024-12-19                出版日期:  2026-05-30      发布日期:  2026-05-30      期的出版日期:  2026-05-30
基金资助: 
福建省自然科学基金项目(2020J05295)
通讯作者:  许珊珊    E-mail:  xushan68@163.com
引用本文:    
张淑颖 连群 李伶俐 曾会勤 宋佳 许珊珊.
DDX3X 基因变异致DDX3X相关神经发育障碍并发中枢性性早熟 1 例报道
[J]. 发育医学电子杂志, 2026, 14(3): 261-265.
Zhang Shuying, Lian Qun, Li Lingli, et al..
A case report of DDX3X-related neurodevelopmental disorder caused by DDX3X variant complicated with central precocious puberty
. Journal of Developmental Medicine(Electronic Version), 2026, 14(3): 261-265.
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http://www.fyyxzz.com/CN/xushan68@163.com  或          http://www.fyyxzz.com/CN/Y2026/V14/I3/261
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