Children's Hospital Boston, Boston, Massachusetts.
Gillette Children's Specialty Healthcare, St. Paul, Minnesota.
J Bone Joint Surg Am. 2020 Oct 21;102(20):1815-1822. doi: 10.2106/JBJS.20.00281.
Deficiency of the radial aspect of the forearm and hand is the most common congenital longitudinal deficiency of the upper limb. Radial longitudinal deficiency is associated with several named syndromes. The purpose of the present study was to explore patterns of radial longitudinal deficiency and thumb hypoplasia in syndromes and to examine the severity of these differences across various syndromes.
Data were collected from the Congenital Upper Limb Differences (CoULD) registry. Congenital differences are classified in the registry with use of the Oberg-Manske-Tonkin (OMT) classification system. Diagnosis of a syndrome by a physician as noted in the CoULD registry was recorded. Thumb deficiency and radial deficiency were classified according to the modified versions of the Blauth criteria and the Bayne and Klug criteria, respectively.
We identified 259 patients with 383 affected limbs with radial deficiency. Eighty-three of these patients had a diagnosed syndrome. The severity of radial deficiency was correlated with the severity of thumb deficiency. The Kendall tau coefficient indicated significant correlation between radial severity and thumb severity (tau = 0.49 [95% confidence interval = 0.40 to 0.57]; p < 0.05). Subjects with a syndrome were twice as likely to have bilateral deficiency and 2.5 times more likely to have both radial and thumb deficiency compared with subjects without a syndrome. Subjects with VACTERL syndrome (vertebral defects, anal atresia, cardiac anomalies, tracheoesophageal fistula, renal anomalies, and limb defects) had patterns of thumb and radial deficiency similar to the general cohort, whereas subjects with Holt-Oram syndrome, TAR (thrombocytopenia absent radius) syndrome, and Fanconi anemia demonstrated varied presentations of thumb and radial deficiency.
The present study investigated the characteristics of patients with radial longitudinal deficiency and thumb hypoplasia. Our results support the findings of previous research correlating the severity of radial deficiency with the severity of thumb deficiency. Furthermore, we identified characteristic features of patients with radial longitudinal deficiency and associated syndromes.
前臂和手部的桡侧部分缺失是上肢最常见的先天性纵向缺失。桡侧纵向缺失与几种命名的综合征有关。本研究的目的是探讨综合征中桡侧纵向缺失和拇指发育不全的模式,并检查这些差异在不同综合征中的严重程度。
数据来自先天性上肢差异(CoULD)登记处。在登记处,先天性差异是使用 Oberg-Manske-Tonkin(OMT)分类系统进行分类的。CoULD 登记处记录了医生诊断的综合征。拇指缺失和桡侧缺失分别根据改良的 Blauth 标准和 Bayne 和 Klug 标准进行分类。
我们确定了 259 名患者,383 只受累肢体存在桡侧缺失。其中 83 名患者患有诊断出的综合征。桡侧缺失的严重程度与拇指缺失的严重程度相关。Kendall tau 系数表明桡侧严重程度与拇指严重程度之间存在显著相关性(tau = 0.49 [95%置信区间 = 0.40 至 0.57];p < 0.05)。与无综合征的患者相比,患有综合征的患者双侧缺失的可能性增加了一倍,同时患有桡侧和拇指缺失的可能性增加了 2.5 倍。VACTERL 综合征(椎体缺陷、肛门闭锁、心脏异常、气管食管瘘、肾脏异常和肢体缺陷)患者的拇指和桡侧缺失模式与一般队列相似,而 Holt-Oram 综合征、TAR(桡骨缺失伴血小板减少)综合征和范可尼贫血患者的拇指和桡侧缺失表现出不同的特征。
本研究调查了桡侧纵向缺失和拇指发育不全患者的特征。我们的结果支持先前研究的发现,即桡侧缺失的严重程度与拇指缺失的严重程度相关。此外,我们确定了具有桡侧纵向缺失和相关综合征的患者的特征。