病例报告:NFIX相关的马兰综合征的眼部表现
Altuğ Ay1, Florian H Guillot2, Andrew R Carey2
1School of Medicine, Bahçeşehir University, Istanbul, Turkey.
Ophthalmic genetics
|March 24, 2025
概括
马兰综合征是一种过度生长障碍,可导致视力缩导致视力丧失. 基因检测证实了最初被诊断为索托斯综合征的患者的马兰综合征,强调了它对罕见疾病的重要性.
科学领域:
- 遗传学 是一个遗传学.
- 眼科医生 眼科 眼科
- 儿科 儿科 儿科
背景情况:
- 马兰综合征是一种罕见的过度生长疾病,与致病性NFIX基因变异相关.
- 关键特征包括巨头,独特的面部特征和智力障碍.
- 在这种情况下,眼科表现越来越多地被认可.
研究的目的:
- 报告一个具有重大眼科发现的马兰综合征病例.
- 根据遗传和临床表现,区分马兰综合征和索托斯综合征.
- 强调基因检测在诊断综合征性过度生长障碍中的作用.
主要方法:
- 一个年轻男性的临床病例呈现,视力逐渐丧失.
- 眼科检查,包括视敏度评估和成像.
- 基因检测用于识别致病变体.
主要成果:
- 患者出现发育迟缓,和逐渐失明.
- 眼科发现包括双边视力缩和视力敏度降低.
- 遗传分析显示,一种异合致病原性NFIX变体,证实了马兰综合征.
结论:
- 在患有过度生长表型的患者视力缩的差异诊断中应考虑马兰综合征.
- 基因检测对于准确诊断和区分马兰综合征与其他过度生长障碍,如索托斯综合征至关重要.
- 这一案例凸显了识别Malan综合征中相关的眼科特征的重要性.
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