Arthrogryposis is a descriptive term, not a specific disease entity: Escobar Syndrome is an example.

IF 2.6 4区 医学 Q2 Medicine Minerva pediatrica Pub Date : 2024-02-01 Epub Date: 2020-06-12 DOI:10.23736/S2724-5276.20.05796-5
Ali Al Kaissi, Sergey Ryabykh, Polina Ochirova, Sami Bouchoucha, Vladimir Kenis, Mohammad Shboul, Rudolf Ganger, Franz Grill, Susanne G Kircher
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Abstract

Background: Children born with multiple congenital contractures have been almost always given the diagnosis of arthrogryposis multiplex congenita. Arthrogryposis is a descriptive term, not a specific disease entity. A heterogeneous group of conditions associated with multiple congenital joint contractures (mostly syndromic) should be considered.

Methods: The records of seven children (four boys and three girls aged 6 months - 11 years) of different ethnic origins have been included in this study. The constellation of specific craniofacial dysmorphic features, spine malformation complex, and appendicular skeletal abnormalities in addition to camptodactyly, talipes equinovarus and rocker-bottom feet were a cluster of malformation complex encountered in our patients. Via comprehensive clinical and imaging study (3D reconstruction CT scan), definite diagnosis of Escobar Syndrome has been approached.

Results: The clinical and imaging phenotype was the key factor towards etiological understanding, treatment and genotype confirmation. We identified compound heterozygous mutations (c.459dupA [p.Val154Serfs*24] and c.794T>G [p.Leu265Serfs*24] of the CHRNG gene in four patients. Bilateral flexion contractures of the knees have been treated by using Iliazarov external fixator. Simultaneous corrections of scoliosis have been achieved by applying either dual traditional growing rods or single growing rods.

Conclusions: The clinical and radiological phenotypic characterizations are the fundamental tool in differentiating Escobar from other forms of multiple contractures. The aim of this study are three folds, firstly to demonstrate the importance of detecting the etiological understanding in children presented with multiple contractures, secondly to refute the general conception among the vast majority of pediatricians and orthopedic surgeons that arthrogryposis multiplex is a diagnostic entity. And thirdly, we were able to detect severe spine deformity via 3D reconstruction CT scan, namely unsegmented posterior spinal bar.

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关节突眼症是一个描述性术语,而不是一种特定的疾病实体:埃斯科巴综合征就是一个例子。
背景:先天性多发挛缩症患儿几乎总是被诊断为先天性多关节畸形。关节挛缩症是一个描述性术语,而不是一种特定的疾病实体。应考虑与多发性先天性关节挛缩(多为综合征)相关的一组异质性疾病:本研究收集了 7 名不同种族儿童(4 男 3 女,年龄在 6 个月至 11 岁之间)的病历。除了外八字腿、马蹄内翻足和摇椅底足之外,患者还伴有特殊的颅面畸形特征、脊柱畸形综合征和附肢骨骼异常。通过全面的临床和影像学研究(三维重建 CT 扫描),最终确诊为埃斯科巴综合征:临床和影像学表型是了解病因、治疗和确认基因型的关键因素。我们在四名患者中发现了 CHRNG 基因的复合杂合突变(c.459dupA [p.Val154Serfs*24] 和 c.794T>G [p.Leu265Serfs*24])。使用 Iliazarov 外固定器治疗了双侧膝关节屈曲挛缩。通过使用传统的双生长棒或单生长棒,脊柱侧弯得到了同时矫正:临床和放射学表型特征是区分埃斯科巴和其他形式的多发性挛缩的基本工具。本研究的目的有三个方面:首先,证明了对患有多发性挛缩的儿童进行病因学检查的重要性;其次,驳斥了绝大多数儿科医生和骨科医生认为多发性关节畸形是一种诊断实体的普遍观念。第三,我们能够通过三维重建CT扫描发现严重的脊柱畸形,即脊柱后方无节段。
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来源期刊
Minerva pediatrica
Minerva pediatrica PEDIATRICS-
CiteScore
2.70
自引率
3.80%
发文量
1
审稿时长
>12 weeks
期刊介绍: Minerva Pediatrica publishes scientific papers on pediatrics, neonatology, adolescent medicine, child and adolescent psychiatry and pediatric surgery. Manuscripts may be submitted in the form of editorials, original articles, review articles, special articles, letters to the Editor and guidelines. The journal aims to provide its readers with papers of the highest quality and impact through a process of careful peer review and editorial work.
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