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盲人摸象:认识1型强直性肌营养不良的多系统症状

The blind men and the elephant: recognising the multisystem symptoms of myotonic dystrophy type 1.

作者信息

Leeuwenberg Kristofoor E, Bruijnes Johanna E, Karnebeek Llse, Smulders Fran, Altena-Rensen Sandra, Gorissen-Brouwers Caroline M L, Klinkenberg Sylvia, Faber Catharina G, Braakman Hilde, Mul Karlien

机构信息

Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud Research Institute for Medical Innovation, Nijmegen, The Netherlands.

Department of Neurology, School of Mental Health and Neuroscience, Maastricht University Medical Center+, Maastricht, The Netherlands.

出版信息

Orphanet J Rare Dis. 2025 Aug 13;20(1):427. doi: 10.1186/s13023-025-03920-z.

Abstract

Although myotonic dystrophy type 1 (DM1) is named after its characteristic muscle symptoms, it is in fact a multisystem disorder that can affect many different organs. It is therefore not surprising that this disease can manifest with a myriad of symptoms, depending on the organs involved. The age of onset and severity of symptoms vary widely. Diagnostic delays of more than ten years are common and it's not unusual for an entire family to be diagnosed only after the birth of a child with a severe phenotype. Knowledge of the spectrum of possible symptoms in DM1 can aid clinicians to recognise this disorder, thereby preventing unnecessary diagnostic delay and facilitating early treatment of disease complications. Here, we present an overview of the potential symptoms of DM1 at different ages, with the aim of raising awareness among healthcare professionals about the recognition of this disabling disease.

摘要

虽然1型强直性肌营养不良症(DM1)是以其特征性的肌肉症状命名的,但它实际上是一种多系统疾病,可影响许多不同器官。因此,这种疾病会因受累器官的不同而表现出无数症状也就不足为奇了。症状的发病年龄和严重程度差异很大。超过十年的诊断延迟很常见,而且通常是在一个患有严重表型的孩子出生后,整个家族才被诊断出来。了解DM1可能出现的症状范围有助于临床医生识别这种疾病,从而避免不必要的诊断延迟,并促进对疾病并发症的早期治疗。在此,我们概述了DM1在不同年龄段可能出现的症状,目的是提高医疗保健专业人员对这种致残性疾病的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af27/12351900/1c3f7111580d/13023_2025_3920_Fig2_HTML.jpg

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