病例报告:由TAD病变引起的儿科巨症的管理,X链接的巨症
Manuela Caruso1, Diego Mazzatenta2,3, Sofia Asioli2,3
1Department of Pediatrics, Azienda Policlinico Università di Catania, Catania, Italy.
Frontiers in endocrinology
|March 14, 2024
概括
链接X型巨症 (X-LAG) 是一种罕见的遗传疾病,由于GPR101基因过度表达,导致巨症. 这项研究详细介绍了患者的旅程,强调了这种复杂疾病的新治疗方法.
科学领域:
- 内分泌学 在内分泌学.
- 遗传学 是一个遗传学.
- 在瘤学瘤学.
背景情况:
- 链接到X的巨症 (X-LAG) 是一种罕见的疾病,其特征是过度生长,与分泌生长激素 (GH) 和前性蛋白的垂体瘤有关.
- 这种情况是由Xq26.3染色体的重复引起的,导致GPR101基因的过度表达,这是GH和益生菌素的强有力的刺激剂.
- 通常情况下,GPR101位于它自己的拓关联域 (TAD) 中,与监管元素隔绝.
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