Wojtara Magda Sara, Kang Jayne, Zaman Mohammed
Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, United States.
Department of Health Sciences, Queen's University, Kingston, ON, Canada.
JMIR Dermatol. 2023 Oct 5;6:e48413. doi: 10.2196/48413.
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.
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.
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.
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.
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.
先天性毛细血管扩张性红斑(CTE),也称为布卢姆综合征,是一种罕见的常染色体隐性疾病,其特征为身高低于平均水平、面部狭窄、身体暴露于阳光下的部位出现红色皮疹以及患癌风险增加。CTE是众多与DNA修复缺陷相关的遗传性皮肤病和光皮肤病之一。CTE由BLM基因发生的突变引起,该突变导致染色体异常断裂。
我们旨在分析关于CTE的现有文献,以进一步深入了解其遗传情况、临床表现谱以及该疾病的管理。此外,概述了当前研究中的差距以及利用人工智能简化CTE临床诊断和管理的情况。
在PubMed、DOAJ和Scopus上进行文献检索,使用“先天性毛细血管扩张性红斑”、“布卢姆综合征”和“布卢姆 - 托雷 - 马查切克”等检索词。由于当前文献有限,本综述考虑了2000年1月至2023年1月发表的研究。共分析了来自文献的49个来源。
通过本次范围综述,研究人员能够识别出几篇关注布卢姆综合征的出版物。一些常见的主题领域包括CTE的遗传、CTE的临床表现以及CTE的管理。此外,关于罕见疾病的文献显示了人工智能在理解和治疗方面的潜在进展。未来的研究应解决表现异质性的原因,并研究CTE及类似表现综合征的潜在治疗候选药物。
本综述阐明了CTE发病过程中潜在分子靶点或致病途径的当前进展以及包括红斑、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该领域的创新,特别是在利用人工智能(包括机器学习和深度学习)诊断和临床管理CTE等罕见疾病方面。