成人综合症:挑战、机遇和前景:通过对四名患有科斯特洛综合征的成人的描述来说明。

IF 1.1 4区 生物学 Medizinische Genetik Pub Date : 2024-06-06 eCollection Date: 2024-06-01 DOI:10.1515/medgen-2024-2023
Ariane Schmetz, Maria Juliana Ballesta-Martínez, Bertrand Isidor, Ana Berta Sousa, Dagmar Wieczorek, Nuria C Bramswig
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引用次数: 0

摘要

临床遗传学家和综合征学家历来专注于鉴定儿童的综合征。然而,人们越来越认识到描述成人表型的必要性。本文概述了罕见遗传综合征成年后的表型演变,阐明了其挑战、机遇和未来前景。文章描述了四名科斯特洛综合征成人患者的临床表型,以说明这些方面的问题。来自四名患者的表型和基因型数据拓宽了科斯特洛综合征在成年期的发病范围,并强调了神经认知结果的高度可变性。临床数据与之前的研究结果和已确定的基因型-表型相关性一致。有趣的是,其中两人患有复发性癌症(膀胱癌和神经母细胞瘤)。进一步的研究势在必行,以便为咨询和管理提供可靠的信息,从而全面了解罕见综合征疾病的演变特征以及成年后的特殊健康问题。
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Adult syndromology: challenges, opportunities and perspectives: Illustrated by the description of four adults with Costello syndrome.

Clinical geneticists and syndromologists have traditionally focused on identifying syndromes in children. However, there is a growing acknowledgment of the need to describe adult phenotypes. This article provides an overview of the evolving phenotypes of rare genetic syndromes into adulthood, elucidating its challenges, opportunities, and future perspectives. The clinical phenotypes of four adults with Costello syndrome are described to illustrate these aspects. Phenotypic and genotypic data from four individuals broaden the spectrum of Costello syndrome in adulthood and highlight the high variability in neurocognitive outcome. The clinical data align with previous findings and established genotype-phenotype correlations. Interestingly, two individuals presented with recurrent cancers (bladder cancer and neuroblastoma). Further studies are imperative to provide reliable information for counselling and management to enable comprehensive understanding of the evolving features of rare syndromic diseases and special health issues into adulthood.

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来源期刊
Medizinische Genetik
Medizinische Genetik GENETICS & HEREDITY-
自引率
9.10%
发文量
48
期刊介绍: medizinischegenetik is a scientific journal that is owned and published by the German Society of Human Genetics e.V. since 1989. The journal was founded by Prof. Jan Murken, München. Self-published until 2006, from 2007-2019 published at Springer Verlag and since 2020 at De Gruyter. medizinischegenetik serves education and training among colleagues, the interdisciplinary exchange of knowledge in all areas of human genetics in clinics, practice, research and teaching. Each issue of the quarterly journal deals with a focus that provides a comprehensive overview of current developments in specific clinical pictures, technical developments and therapeutic approaches. All reviews are written in English language. The journal thus creates a platform for the international exchange of knowledge and increased awareness of German research activities in the scientific community. In addition, medizinischegenetik contains information on activities in its own subject in the German-language section. This includes conference reports, association announcements, personnel matters, statements and guidelines. With health policy questions, historical retrospectives and comments on current developments, the profession takes a stand on human genetic issues in Germany, Austria and Switzerland.
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