一名中国婴儿患有复合异性SLC26A3突变的先天化物腹
Qian Li1,2, Jing Wang1,2, Ruixian Zang2
1Department of Pediatric Nephrology and Rheumatism and Immunology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250021, P.R. China.
BMC pediatrics
|May 4, 2024
概括
先天性性腹 (CCD) 是一种遗传性疾病,由于SLC26A3基因突变,导致严重的婴儿腹和电解质失衡. 对于患有长期腹的婴儿和母亲多水的婴儿,早期考虑CCD至关重要.
科学领域:
- 遗传学 遗传学 是一个
- 儿科 儿科 儿科
- 胃肠病学 胃肠病学
背景情况:
- 先天性化物腹 (CCD) 是一种自身相对递归性疾病.
- 它是由溶解物载体家族26成员3 (SLC26A3) 基因的突变引起的.
- 在婴儿中,CCD会导致分泌性腹和危及生命的电解质障碍.
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