伪巴特特综合征:一种CFTR相关的疾病?
Noelia Rodriguez Mier1, Virginie Antoons2, Senne Cuyx1
1Department of Pediatrics, Pediatric Pulmonology, University Hospital of Leuven, Leuven, Belgium; Department of Development and Regeneration, Woman and Child Unit, CF Research Lab, KU Leuven, Leuven, Belgium.
概括
伪巴特特综合征可能是囊性纤维化转膜导电调节器相关障碍 (CFTR-RD) 的罕见表现. 功能性CFTR测试对于中等汗液化物水平的婴儿的准确诊断至关重要.
科学领域:
- 儿科 儿科 儿科
- 遗传学 是一个遗传学.
- 内分泌学 在内分泌学.
背景情况:
- 囊性纤维化 (CF) 新生儿查 (CF-NBS) 识别有风险的婴儿.
- 伪巴特特综合征 (PBS) 是一种罕见的疾病,症状重叠.
- 与CFTR相关的疾病 (CFTR-RD) 包含CFTR基因变异的疾病,但不是经典的CF.
研究的目的:
- 报告 CFTR-RD 在婴儿中呈现为 PBS 的病例.
- 为了突出CFTR-RD在NBS之后的诊断挑战.
- 强调功能CFTR测试的实用性.
主要方法:
- 一个14个月大的男孩患有CF携带者身份和PBS症状的案例介绍.
- 最初的评估包括汗水化物测试.
- 对CFTR突变的遗传分析.
- 对CFTR功能进行直肠器官形态分析 (ROMA).
主要成果:
- 婴儿被诊断出CFTR-RD尽管最初的CF工作是负面的.
- 中介性汗液化物和已识别的CFTR突变.
- 罗马证实了CFTR功能障碍.
- PBS症状与CFTR-RD有关.
结论:
- PBS可能是CFTR-RD的罕见表现.
- 功能性CFTR测试 (ROMA) 有助于诊断CFTR-RD.
- 患有CFTR-RD的婴儿需要在CF中心进行专门的随访.
- 这种情况不应该被标记为CF NBS故障.
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