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先天性糖基化障碍的治疗:概述。

Treatment of congenital disorders of glycosylation: An overview.

机构信息

Unidade de Bioquímica Genética, Serviço de Genética Laboratorial, Centro de Genética Médica, Clínica de Genética e Patologia, Centro Hospitalar Universitário de Santo António, Unidade Local de Saúde de Santo António, Porto, Portugal; Unit for Multidisciplinary Research in Biomedicine, ICBAS, UP, Porto, Portugal; Centro Referência Doenças Hereditárias do Metabolismo, Centro Hospitalar Universitário de Santo António, Unidade Local de Saúde de Santo António, Porto, Portugal.

Center for Metabolic Diseases, University Hospital Gasthuisberg, KU Leuven, Leuven, Belgium.

出版信息

Mol Genet Metab. 2024 Sep-Oct;143(1-2):108567. doi: 10.1016/j.ymgme.2024.108567. Epub 2024 Aug 18.

Abstract

While the identification and diagnosis of congenital disorders of glycosylation (CDG) have rapidly progressed, the available treatment options are still quite limited. Mostly, we are only able to manage the disease symptoms rather than to address the underlying cause. However, recent years have brought about remarkable advances in treatment approaches for some CDG. Innovative therapies, targeting both the root cause and resulting manifestations, have transitioned from the research stage to practical application. The present paper aims to provide a detailed overview of these exciting developments and the rising concepts that are used to treat these ultra-rare diseases.

摘要

尽管先天性糖基化障碍(CDG)的鉴定和诊断已经取得了快速进展,但可用的治疗选择仍然相当有限。我们大多只能管理疾病症状,而不能解决根本原因。然而,近年来,一些 CDG 的治疗方法取得了显著进展。针对根本原因和由此产生的表现的创新疗法已经从研究阶段过渡到实际应用。本文旨在详细介绍这些令人兴奋的发展以及用于治疗这些超罕见疾病的新兴概念。

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