盲人和大象:1型强直性肌营养不良多系统症状的认识。

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Kristofoor E Leeuwenberg, Johanna E Bruijnes, Llse Karnebeek, Fran Smulders, Sandra Altena-Rensen, Caroline M L Gorissen-Brouwers, Sylvia Klinkenberg, Catharina G Faber, Hilde Braakman, Karlien Mul
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引用次数: 0

摘要

虽然1型肌强直性营养不良症(DM1)是以其特有的肌肉症状命名的,但实际上它是一种多系统疾病,可以影响许多不同的器官。因此,这种疾病可以表现出无数的症状,这并不奇怪,这取决于所涉及的器官。发病的年龄和症状的严重程度差别很大。诊断延迟10年以上是很常见的,整个家庭只有在孩子出生后才被诊断出患有严重的表型,这并不罕见。了解DM1的可能症状谱可以帮助临床医生识别这种疾病,从而防止不必要的诊断延误并促进疾病并发症的早期治疗。在这里,我们概述了DM1在不同年龄的潜在症状,目的是提高医疗保健专业人员对这种致残疾病的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The blind men and the elephant: recognising the multisystem symptoms of myotonic dystrophy type 1.

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.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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