Congenital Telangiectatic Erythema: Scoping Review.

Q3 Medicine JMIR dermatology Pub Date : 2023-10-05 DOI:10.2196/48413
Magda Sara Wojtara, Jayne Kang, Mohammed Zaman
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Abstract

Background: Congenital telangiectatic erythema (CTE), also known as Bloom syndrome, is a rare autosomal recessive disorder characterized by below-average height, a narrow face, a red skin rash occurring on sun-exposed areas of the body, and an increased risk of cancer. CTE is one of many genodermatoses and photodermatoses associated with defects in DNA repair. CTE is caused by a mutation occurring in the BLM gene, which causes abnormal breaks in chromosomes.

Objective: We aimed to analyze the existing literature on CTE to provide additional insight into its heredity, the spectrum of clinical presentations, and the management of this disorder. In addition, the gaps in current research and the use of artificial intelligence to streamline clinical diagnosis and the management of CTE are outlined.

Methods: A literature search was conducted on PubMed, DOAJ, and Scopus using search terms such as "congenital telangiectatic erythema," "bloom syndrome," and "bloom-torre-machacek." Due to limited current literature, studies published from January 2000 to January 2023 were considered for this review. A total of 49 sources from the literature were analyzed.

Results: Through this scoping review, the researchers were able to identify several publications focusing on Bloom syndrome. Some common subject areas included the heredity of CTE, clinical presentations of CTE, and management of CTE. In addition, the literature on rare diseases shows the potential advancements in understanding and treatment with artificial intelligence. Future studies should address the causes of heterogeneity in presentation and examine potential therapeutic candidates for CTE and similarly presenting syndromes.

Conclusions: This review illuminated current advances in potential molecular targets or causative pathways in the development of CTE as well as clinical features including erythema, increased cancer risk, and growth abnormalities. Future studies should continue to explore innovations in this space, especially in regard to the use of artificial intelligence, including machine learning and deep learning, for the diagnosis and clinical management of rare diseases such as CTE.

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先天性毛细血管扩张性红斑:范围界定综述。
背景:先天性毛细血管扩张性红斑(CTE),也称为布鲁姆综合征,是一种罕见的常染色体隐性遗传疾病,其特征是身高低于平均水平,面部狭窄,身体阳光照射区域出现红色皮疹,患癌症的风险增加。CTE是许多与DNA修复缺陷相关的遗传性皮肤病和光损伤病之一。CTE是由BLM基因发生突变引起的,该突变会导致染色体异常断裂。目的:我们旨在分析现有的CTE文献,以进一步了解其遗传、临床表现谱和该疾病的治疗。此外,还概述了当前研究以及使用人工智能简化临床诊断和CTE管理方面的差距。方法:在PubMed、DOAJ和Scopus上使用“先天性毛细血管扩张性红斑”、“bloom综合征”和“bloom-torre machacek”等搜索词进行文献检索。由于现有文献有限,本综述考虑了2000年1月至2023年1月发表的研究。对文献中的49个来源进行了分析。结果:通过这篇范围界定综述,研究人员能够确定几篇关注布鲁姆综合征的出版物。一些常见的主题领域包括CTE的遗传、CTE的临床表现和CTE的管理。此外,有关罕见病的文献显示了人工智能在理解和治疗方面的潜在进展。未来的研究应该解决表现异质性的原因,并检查CTE和类似表现综合征的潜在候选治疗方法。结论:这篇综述阐明了CTE发展中潜在分子靶点或致病途径的最新进展,以及包括红斑、癌症风险增加和生长异常在内的临床特征。未来的研究应继续探索这一领域的创新,特别是在使用包括机器学习和深度学习在内的人工智能来诊断和临床管理罕见病(如CTE)方面。
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CiteScore
1.20
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0.00%
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审稿时长
18 weeks
期刊最新文献
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