Clinical presentation and genetics of tricho-rhino-phalangeal syndrome (TRPS) type 1: A single-center case series of 15 patients and seven novel TRPS1 variants

IF 1.6 4区 医学 Q3 GENETICS & HEREDITY
Laura Krogh Herlin , Morten Krogh Herlin , Jenny Blechingberg , Kirsten Rønholt , Lise Graversen , Sigrun A.J. Schmidt , Mette Warming Jørgensen , Michel Bach Hellfritzsch , Jannie Dahl Hald , Signe Sparre Beck-Nielsen , Hans Gjørup , Brian Nauheimer Andersen , Pernille Axél Gregersen , Mette Sommerlund
{"title":"Clinical presentation and genetics of tricho-rhino-phalangeal syndrome (TRPS) type 1: A single-center case series of 15 patients and seven novel TRPS1 variants","authors":"Laura Krogh Herlin ,&nbsp;Morten Krogh Herlin ,&nbsp;Jenny Blechingberg ,&nbsp;Kirsten Rønholt ,&nbsp;Lise Graversen ,&nbsp;Sigrun A.J. Schmidt ,&nbsp;Mette Warming Jørgensen ,&nbsp;Michel Bach Hellfritzsch ,&nbsp;Jannie Dahl Hald ,&nbsp;Signe Sparre Beck-Nielsen ,&nbsp;Hans Gjørup ,&nbsp;Brian Nauheimer Andersen ,&nbsp;Pernille Axél Gregersen ,&nbsp;Mette Sommerlund","doi":"10.1016/j.ejmg.2024.104937","DOIUrl":null,"url":null,"abstract":"<div><p>Tricho-rhino-phalangeal syndrome (TRPS) is a rare malformation syndrome characterized by distinctive facial, ectodermal, and skeletal features. TRPS is divided into TRPS type I/III caused by pathogenic variants in <em>TRPS1</em> and TRPS type II caused by contiguous gene deletions also spanning <em>EXT1</em> and <em>RAD21</em>. Due to its rarity, knowledge of the clinical course of TRPS remains limited.</p><p>Therefore, we collected and characterized a case series of 15 TRPS type I patients (median age at diagnosis 15 [interquartile range: 10–18] years, 11 females [73%]) seen at Aarhus University Hospital, Denmark, with a median follow-up period of 10 years. We estimated a minimum point prevalence of 0.5 in 100,000 (95% CI: 0.3–0.8 per 100,000) persons.</p><p>Common craniofacial features included fine and sparse hair with a high anterior hairline, eyebrows with lateral thinning and a thicker medial part, prominent ears, a bulbous nose tip with small nasal alae, a low-hanging, and often wide columella, and a long philtrum with a thin upper vermillion. Specific skeletal features included short stature and deviating and short fingers with cone-shaped epiphyses and shortened metacarpals on radiographs. The most significant morbidity of the cohort was joint complaints, which were reported by all patients, often already before the TRPS diagnosis was established.</p><p>We identified ten different <em>TRPS1</em> variants including both frameshift/nonsense, missense, and splice-site variants, including seven variants not previously reported in the literature. In accordance with previous literature, no genotype-phenotype correlation was identified.</p><p>The clinical trajectories were heterogeneous involving pediatrics, dermatology, orthopedic surgery, clinical genetics, and/or odontology, emphasizing that close multidisciplinary collaboration is essential for early diagnosis of TRPS and to ensure proper and timely patient care and counseling.</p></div>","PeriodicalId":11916,"journal":{"name":"European journal of medical genetics","volume":"69 ","pages":"Article 104937"},"PeriodicalIF":1.6000,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1769721224000296/pdfft?md5=bd46259febf30bd57bbedec11df65999&pid=1-s2.0-S1769721224000296-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of medical genetics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1769721224000296","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Tricho-rhino-phalangeal syndrome (TRPS) is a rare malformation syndrome characterized by distinctive facial, ectodermal, and skeletal features. TRPS is divided into TRPS type I/III caused by pathogenic variants in TRPS1 and TRPS type II caused by contiguous gene deletions also spanning EXT1 and RAD21. Due to its rarity, knowledge of the clinical course of TRPS remains limited.

Therefore, we collected and characterized a case series of 15 TRPS type I patients (median age at diagnosis 15 [interquartile range: 10–18] years, 11 females [73%]) seen at Aarhus University Hospital, Denmark, with a median follow-up period of 10 years. We estimated a minimum point prevalence of 0.5 in 100,000 (95% CI: 0.3–0.8 per 100,000) persons.

Common craniofacial features included fine and sparse hair with a high anterior hairline, eyebrows with lateral thinning and a thicker medial part, prominent ears, a bulbous nose tip with small nasal alae, a low-hanging, and often wide columella, and a long philtrum with a thin upper vermillion. Specific skeletal features included short stature and deviating and short fingers with cone-shaped epiphyses and shortened metacarpals on radiographs. The most significant morbidity of the cohort was joint complaints, which were reported by all patients, often already before the TRPS diagnosis was established.

We identified ten different TRPS1 variants including both frameshift/nonsense, missense, and splice-site variants, including seven variants not previously reported in the literature. In accordance with previous literature, no genotype-phenotype correlation was identified.

The clinical trajectories were heterogeneous involving pediatrics, dermatology, orthopedic surgery, clinical genetics, and/or odontology, emphasizing that close multidisciplinary collaboration is essential for early diagnosis of TRPS and to ensure proper and timely patient care and counseling.

三叉神经头综合征(TRPS)1 型的临床表现和遗传学:15 例患者和 7 个新型 TRPS1 变体的单中心病例系列研究
三鼻-头盖骨综合征(TRPS)是一种罕见的畸形综合征,以独特的面部、外胚层和骨骼特征为特征。TRPS分为由TRPS1致病变异引起的TRPS I/III型和由同样跨越EXT1和RAD21的连续基因缺失引起的TRPS II型。因此,我们收集了丹麦奥胡斯大学医院接诊的 15 例 TRPS I 型患者(诊断时的中位年龄为 15 [四分位距:10-18]岁,其中 11 例为女性 [73%]),并对其进行了特征性分析,中位随访时间为 10 年。常见的颅面特征包括:头发稀疏,前发际线较高;眉毛外侧稀疏,内侧较浓密;耳朵突出;鼻尖凸出,鼻翼较小;鼻梁低垂,通常较宽;咽鼓管较长,上部朱砂较薄。具体的骨骼特征包括身材矮小、手指偏斜和短小,X 光片显示手指骨骺呈锥形,掌骨缩短。所有患者都有关节不适的症状,这些症状往往在TRPS诊断确立之前就已出现。我们发现了10种不同的TRPS1变异,包括移帧/缺义、错义和剪接位点变异,其中7种变异以前未在文献中报道过。这些患者的临床轨迹各不相同,涉及儿科、皮肤科、整形外科、临床遗传学和/或口腔科,这强调了多学科密切协作对于早期诊断 TRPS 以及确保正确及时的患者护理和咨询至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
4.10
自引率
0.00%
发文量
193
审稿时长
66 days
期刊介绍: The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信