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先天性马蹄内翻足与 22q11.2 缺失综合征相关:一项观察性研究。

Club foot in association with the 22q11.2 deletion syndrome: An observational study.

机构信息

Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.

Division of Human Genetics and 22q and You Center, The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania.

出版信息

Am J Med Genet A. 2018 Oct;176(10):2135-2139. doi: 10.1002/ajmg.a.40649.

Abstract

The 22q11.2 Deletion Syndrome (22q11.2DS) occurs in ~1:3,000-6,000 individuals. Features less typically associated with 22q11.2DS, such as orthopedic manifestations, may be overlooked or may not lead to appropriate diagnostic testing. Club foot has a general population prevalence of ~1:1,000 and has been occasionally described in association with 22q11.2DS. Our hypothesis is that the prevalence of club foot is higher in patients with 22q11.2DS. We performed a retrospective review in two specialized 22q11.2DS centers to determine the prevalence of club foot. "True club foot" requires treatment (either conservative or surgical), therefore we only included those patients with proof of treatment. We investigated whether congenital heart disease (CHD) and/or cleft palate were associated with the presence of club foot within 22q11.2DS. The records of 1,466 patients were reviewed. Of these, 48 (3.3%) had confirmation of club foot (95% Confidence Interval: 2.4-4.3): 22 (46%) had a bilateral, 12 (25%) left, and 14 (29%) right club foot. Within our study, neither a CHD and/or a cleft palate were associated with a club foot. The prevalence of club foot in 22q11.2DS is 30 times higher than that observed in the general population. This suggests the diagnosis of club foot, especially in the face of other typically associated abnormalities of 22q11.2DS, should provoke consideration of 22q11.2DS as an underlying diagnosis, particularly in the neonatal setting.

摘要

22q11.2 缺失综合征(22q11.2DS)在约 1:3000-6000 人中发生。一些不太典型的 22q11.2DS 相关特征,如骨科表现,可能会被忽视,或者不会导致进行适当的诊断性检查。马蹄内翻足在普通人群中的患病率约为 1:1000,偶尔也有报道与 22q11.2DS 有关。我们的假设是,22q11.2DS 患者中马蹄内翻足的患病率更高。我们在两个专门的 22q11.2DS 中心进行了回顾性研究,以确定马蹄内翻足的患病率。“真正的马蹄内翻足”需要治疗(保守或手术),因此我们只包括那些有治疗证明的患者。我们调查了 22q11.2DS 中先天性心脏病(CHD)和/或腭裂是否与马蹄内翻足的存在有关。共回顾了 1466 名患者的记录。其中,48 名(3.3%)患者被确诊为马蹄内翻足(95%置信区间:2.4-4.3%):22 名(46%)为双侧,12 名(25%)为左侧,14 名(29%)为右侧马蹄内翻足。在我们的研究中,CHD 和/或腭裂均与马蹄内翻足无关。22q11.2DS 中马蹄内翻足的患病率是普通人群的 30 倍。这表明,尤其是在存在其他 22q11.2DS 典型相关异常的情况下,马蹄内翻足的诊断应促使考虑 22q11.2DS 作为潜在的诊断,特别是在新生儿期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ef/6221052/e1b26f086fb6/AJMG-176-2135-g001.jpg

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