Predictors of Syndromic Association in Ulnar Polydactyly: Analysis of a Multicenter Congenital Hand Differences Registry in the United States.

IF 2.1 2区 医学 Q2 ORTHOPEDICS
Thomas McQuillan, Hannah Antonellis, Lindley Wall, Suzanne Steinman, Angela Wang, Kim Bjorklund, Mary Claire Manske, Deborah Bohn, Apurva Shah, Andrea Bauer
{"title":"Predictors of Syndromic Association in Ulnar Polydactyly: Analysis of a Multicenter Congenital Hand Differences Registry in the United States.","authors":"Thomas McQuillan, Hannah Antonellis, Lindley Wall, Suzanne Steinman, Angela Wang, Kim Bjorklund, Mary Claire Manske, Deborah Bohn, Apurva Shah, Andrea Bauer","doi":"10.1016/j.jhsa.2025.03.019","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Ulnar polydactyly is one of the most common congenital hand differences in the United States. Prior literature suggests that those with type B (rudimentary) extra digits, patients and caregivers that identify as Black race or skin color, and those with a strong family history of polydactyly are less frequently associated with concomitant genetic syndromes. As race is a social construct, not a biological one, there is a need to quantify the degree of association of other clinical variables with syndromes for risk stratification and testing.</p><p><strong>Methods: </strong>Data from the Congenital Upper Limb Difference (CoULD) Registry were collected and reviewed, involving 10 tertiary hand centers in the United States. Demographic characteristics, morphology, and laterality were analyzed for to their relationship with syndromic and nonsyndromic forms of ulnar polydactyly.</p><p><strong>Results: </strong>Three hundred thirty-four patients (42% female and 63% bilateral) were included in the cohort. Patients with type A (fully formed) polydactyly had an associated syndrome in 21% of cases, compared to 2% of type B ulnar polydactyly. Black patients were less likely to have an associated syndrome than non-Black patients, but with a less strong association than type B morphology. Patients without any family history of upper limb difference were more likely to have an associated syndrome. Bilateral cases were not associated with a syndrome.</p><p><strong>Conclusions: </strong>A high frequency of genetic syndromes was found in patients with type A polydactyly (21%), and these patients were much more likely to have a genetic syndrome than those with rudimentary (type B) digits. Given this strong association with multiorgan genetic syndromes the authors recommend consultation with a genetics specialist for patients with type A ulnar polydactyly for early screening, diagnosis, treatment, and counseling for families.</p><p><strong>Type of study/level of evidence: </strong>Prognostic II.</p>","PeriodicalId":54815,"journal":{"name":"Journal of Hand Surgery-American Volume","volume":" ","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Hand Surgery-American Volume","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jhsa.2025.03.019","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ORTHOPEDICS","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: Ulnar polydactyly is one of the most common congenital hand differences in the United States. Prior literature suggests that those with type B (rudimentary) extra digits, patients and caregivers that identify as Black race or skin color, and those with a strong family history of polydactyly are less frequently associated with concomitant genetic syndromes. As race is a social construct, not a biological one, there is a need to quantify the degree of association of other clinical variables with syndromes for risk stratification and testing.

Methods: Data from the Congenital Upper Limb Difference (CoULD) Registry were collected and reviewed, involving 10 tertiary hand centers in the United States. Demographic characteristics, morphology, and laterality were analyzed for to their relationship with syndromic and nonsyndromic forms of ulnar polydactyly.

Results: Three hundred thirty-four patients (42% female and 63% bilateral) were included in the cohort. Patients with type A (fully formed) polydactyly had an associated syndrome in 21% of cases, compared to 2% of type B ulnar polydactyly. Black patients were less likely to have an associated syndrome than non-Black patients, but with a less strong association than type B morphology. Patients without any family history of upper limb difference were more likely to have an associated syndrome. Bilateral cases were not associated with a syndrome.

Conclusions: A high frequency of genetic syndromes was found in patients with type A polydactyly (21%), and these patients were much more likely to have a genetic syndrome than those with rudimentary (type B) digits. Given this strong association with multiorgan genetic syndromes the authors recommend consultation with a genetics specialist for patients with type A ulnar polydactyly for early screening, diagnosis, treatment, and counseling for families.

Type of study/level of evidence: Prognostic II.

尺侧多指畸形综合征相关性的预测因素:美国多中心先天性手部差异登记的分析。
目的:尺侧多指畸形是美国最常见的先天性手部畸形之一。先前的文献表明,那些B型(基本)外指,患者和护理者被认为是黑人或肤色,以及那些有多指畸形家族史的人很少伴有遗传综合征。由于种族是一种社会结构,而不是生物学结构,因此有必要量化其他临床变量与风险分层和测试综合征的关联程度。方法:收集美国10个三手中心的先天性上肢差异(CoULD)登记处的数据并进行回顾。分析了人口统计学特征、形态学和侧侧性与综合征型和非综合征型尺侧多指畸形的关系。结果:334例患者(42%为女性,63%为双侧)纳入队列。A型(完全成形)尺侧多指畸形患者有相关综合征的病例占21%,而B型尺侧多指畸形患者有相关综合征的病例占2%。黑人患者比非黑人患者更不可能有相关综合征,但与B型形态学的相关性较弱。无上肢差异家族史的患者更容易出现相关综合征。双侧病例不伴有综合征。结论:A型多指畸形患者出现遗传综合征的频率较高(21%),与B型多指畸形患者相比,A型多指畸形患者更容易出现遗传综合征。鉴于这与多器官遗传综合征的强烈关联,作者建议对a型尺多指畸形患者咨询遗传学专家,进行早期筛查、诊断、治疗和家庭咨询。研究类型/证据水平:预后II。
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
3.20
自引率
10.50%
发文量
402
审稿时长
12 weeks
期刊介绍: The Journal of Hand Surgery publishes original, peer-reviewed articles related to the pathophysiology, diagnosis, and treatment of diseases and conditions of the upper extremity; these include both clinical and basic science studies, along with case reports. Special features include Review Articles (including Current Concepts and The Hand Surgery Landscape), Reviews of Books and Media, and Letters to the Editor.
×
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