遗传性葡萄糖-银糖吸收不良表现为高三糖血症和骨髓性神经结症
Malika Goel1, Renu Suthar2, Lesa Dawman2
1Department of Pediatrics, University of California, San Francisco, CA 94158, USA.
Pediatric reports
|September 22, 2025
概括
先天性葡萄糖-银糖吸收不良 (CGGM) 可能会出现罕见的代谢问题,如高甘油三和高胆固醇. 这一案例突出了CGGM不常见的表现,用于早期诊断和管理.
科学领域:
- 遗传学 遗传学 是一个
- 儿科 儿科 儿科
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 先天性葡萄糖-银糖吸收不良 (CGGM) 是一种罕见的遗传疾病,影响营养吸收.
- 典型的症状包括严重的腹和由于葡萄糖和银河糖的吸收不良而无法壮成长.
- 相关的代谢异常在现有文献中没有得到充分记录.
研究的目的:
- 报告一个罕见的CGGM病例与不寻常的代谢表现.
- 强调识别非典型表现的重要性,以便及时诊断.
- 为了解CGGM的遗传基础和临床谱做出贡献.
主要方法:
- 一个四个月大的男婴的临床病例介绍.
- 详细的病史,体检和实验室调查.
- 外体分析以确定导致CGGM的遗传突变.
主要成果:
- 患者出现了发育不良,透性腹,高甘油三血症,高胆固醇血症,高血症和骨髓性骨.
- 外体序列测定揭示了SLC5A1基因中的一种致病突变 (c875G>A,p.Cys292Tyr),证实了CGGM.
- 首次报告了与CGGM相关的过高甘油三和高胆固醇血症.
结论:
- 这一案例强调了CGGM中多样化和不常见的代谢表现的潜力.
- 早期发现像SLC5A1这样的基因突变对于诊断至关重要.
- 对于患有罕见遗传疾病的家庭来说,产前咨询至关重要,以有效地管理未来的怀孕.
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