法布里病早期与晚期治疗干预的益处

Mónica Furlano, Elisabet Ars, Anna Matamala, Vicens Brossa, Joan Martí, Maria Del Prado-Venegas, Jaume Crespi, Esther Roe, Roser Torra
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摘要

背景:法布里病(FD)是一种由GLA基因致病性变异引起的x连锁溶酶体贮积症。杂合子女性患者可能在临床表现上表现出更大的变异性,从无症状到疾病完全发作。由于女性的这种异质性临床表现,FD的诊断通常延迟了十多年,并且开始治疗的最佳时间仍然存在争议。案例演示。在此,我们报告了两名无亲缘关系的女性FD患者携带相同的致病性GLA变体。我们讨论了在疾病的不同阶段启动特异性治疗的意义,有无器官受累(早期与晚期治疗干预)。结论:这些临床病例表明,在FD妇女早期开始特异性治疗可以预防器官受损伤和相关的临床事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Benefits of Early versus Late Therapeutic Intervention in Fabry Disease.

Background: Fabry disease (FD) is an X-linked lysosomal storage disorder caused by pathogenic variants of the GLA gene. Heterozygous female patients may show much more variability in clinical manifestations, ranging from asymptomatic to full-blown disease. Because of this heterogeneous clinical picture in women, the diagnosis of FD has typically been delayed for more than a decade, and the optimal time to initiate treatment remains controversial. Case Presentation. Here, we present two unrelated female patients diagnosed with FD harbouring the same pathogenic GLA variant. We discuss the implications of initiating specific therapy at different stages of the disease, with and without organ involvement (early versus late therapeutic intervention).

Conclusions: These clinical cases suggest that initiating specific treatment at an earlier age in women with FD may prevent organ involvement and associated clinical events.

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