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伴有关节松弛及严重进行性脊柱侧凸的脊椎-骨骺-干骺端发育不良

Spondylo-epi-metaphyseal dysplasia with joint laxity and severe, progressive kyphoscoliosis.

作者信息

Beighton P, Kozlowski K

出版信息

Skeletal Radiol. 1980;5(4):205-12. doi: 10.1007/BF00580591.

DOI:10.1007/BF00580591
PMID:7209574
Abstract
  1. Spondylo-epi-metaphyseal dysplasia with progressive, severe kyphoscoliosis and gross joint laxity is a distinctive entity. The clinical and radiographic manifestations of seven affected children are presented and it is concluded that this disorder is probably more common than previously suspected. Autosomal recessive transmission is likely. 2. Skeletal survey is indicated in all patients with infantile idiopathic scoliosis, kyphosis, or kyphoscoliosis. In this context, radiographic studies of the pelvis may be of great diagnostic value. 3. Referal for expert orthopaedic management is essential for all patients with this disorder, as profound disability with pulmonary and spinal complications may be expected.
摘要
  1. 伴有进行性严重脊柱后凸侧弯和关节明显松弛的脊椎-骨骺-干骺端发育不良是一种独特的病症。本文呈现了7名患病儿童的临床和影像学表现,并得出结论:该疾病可能比之前所怀疑的更为常见。很可能为常染色体隐性遗传。2. 对于所有患有婴儿特发性脊柱侧弯、后凸或脊柱后凸侧弯的患者,均需进行骨骼检查。在此情况下,骨盆的影像学研究可能具有极大的诊断价值。3. 对于所有患有该疾病的患者,转至骨科专家处进行治疗至关重要,因为可能会出现肺部和脊柱并发症导致的严重残疾。

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1
Spondylo-epi-metaphyseal dysplasia with joint laxity and severe, progressive kyphoscoliosis.伴有关节松弛及严重进行性脊柱侧凸的脊椎-骨骺-干骺端发育不良
Skeletal Radiol. 1980;5(4):205-12. doi: 10.1007/BF00580591.
2
Spondylo-epimetaphyseal dysplasia with joint laxity and severe kyphoscoliosis in an Italian girl.一名意大利女孩患有关节松弛和严重脊柱侧凸的脊椎骨骺发育不良。
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Radiographic features of spondylo-epimetaphyseal dysplasia with joint laxity and progressive kyphoscoliosis. Review of 19 cases.伴有关节松弛和进行性脊柱侧凸的脊椎骨骺发育异常的影像学特征。19例病例回顾
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Spondylo-epimetaphyseal dysplasia with joint laxity and severe, progressive kyphoscoliosis. A potentially lethal dwarfing disorder.伴有关节松弛和严重进行性脊柱侧凸的脊椎骨骺发育不良。一种具有潜在致命性的侏儒症。
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[Oligomeganephronia associated with congenital eye and skeletal abnormalities].[与先天性眼部和骨骼异常相关的少肾单位肾发育不全]
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Surgical treatment of atlantoaxial dysplasia and scoliosis in spondyloepiphyseal dysplasia congenita: A case report.先天性脊椎骨骺发育不良中寰枢椎发育不良和脊柱侧弯的外科治疗:一例报告。
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本文引用的文献

1
[Diastrophic nanism].[畸形性侏儒症]
Presse Med (1893). 1960 Nov 23;68:1977-80.
2
Forms of dwarfism recognizable at birth.出生时即可识别的侏儒症类型。
Clin Orthop Relat Res. 1971 May;76:150-9. doi: 10.1097/00003086-197105000-00022.
3
Orthopaedic management of dwarfisms recognizable at birth.出生时可识别的侏儒症的骨科治疗
一名患有埃勒斯-当洛综合征样脊椎骨骺发育异常的中国儿童的新基因突变:病例报告。
Front Pediatr. 2022 Dec 21;10:1073748. doi: 10.3389/fped.2022.1073748. eCollection 2022.
4
Unique Growing Rod Treatment with Prior Foundation Surgery for Spondylo-Epi-Metaphyseal Dysplasia with Severe Kyphoscoliosis: A Case Report.
Spine Surg Relat Res. 2019 Dec 3;4(3):284-286. doi: 10.22603/ssrr.2019-0077. eCollection 2020.
5
Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)- and Spondylodysplastic-EDS-.严重的外周关节松弛是脊柱骨骺发育不良-埃勒斯-当洛斯综合征(EDS)和脊柱骨骺发育不良-EDS 型的一个独特临床特征。
Genes (Basel). 2019 Oct 12;10(10):799. doi: 10.3390/genes10100799.
6
Spondyloepimetaphysial Dysplasia with Joint Laxity in Three Siblings with Mutations.三例携带突变的同胞患伴关节松弛的脊椎骨骺发育异常
Mol Syndromol. 2017 Nov;8(6):303-307. doi: 10.1159/000479672. Epub 2017 Sep 7.
7
Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel mutations.通过对两名携带两个新突变的复合杂合子姐妹的皮肤成纤维细胞进行全转录组表达谱分析,深入了解半乳糖基转移酶II(GalT-II)缺乏症的病因病理。
Mol Genet Metab Rep. 2014 Nov 20;2:1-15. doi: 10.1016/j.ymgmr.2014.11.005. eCollection 2015 Mar.
8
Biosynthesis of glycosaminoglycans: associated disorders and biochemical tests.糖胺聚糖的生物合成:相关疾病及生化检测
J Inherit Metab Dis. 2016 Mar;39(2):173-88. doi: 10.1007/s10545-015-9903-z. Epub 2015 Dec 21.
9
Defective initiation of glycosaminoglycan synthesis due to B3GALT6 mutations causes a pleiotropic Ehlers-Danlos-syndrome-like connective tissue disorder.由于 B3GALT6 突变导致糖胺聚糖合成起始缺陷,引起多系统的埃勒斯-当洛斯综合征样结缔组织疾病。
Am J Hum Genet. 2013 Jun 6;92(6):935-45. doi: 10.1016/j.ajhg.2013.04.016. Epub 2013 May 9.
10
Synophyrs, curly eyelashes and Ptyrigium colli in a girl with Desbuquois dysplasia: a case report and review of the literature.一名患有德斯布瓦发育不全的女孩出现睑裂狭小、卷曲睫毛和蹼状颈:病例报告及文献复习
Cases J. 2009 Sep 15;2:7873. doi: 10.4076/1757-1626-2-7873.
Bull Hosp Joint Dis. 1970 Apr;31(1):27-30.
4
[Metatrophic dwarfism].
Arch Kinderheilkd. 1966 Feb;173(3):211-26.
5
Metacarpophalangeal pattern profiles in the evaluation of skeletal malformations.掌指骨形态轮廓在骨骼畸形评估中的应用
Radiology. 1972 Jul;104(1):1-11. doi: 10.1148/104.1.1.
6
Dysplasia spondylo-epiphysealis congenita Spranger-Wiedemann. A critical analysis.先天性脊椎骨骺发育异常Spranger-Wiedemann型。批判性分析。
Australas Radiol. 1977 Sep;21(3):260-80. doi: 10.1111/j.1440-1673.1977.tb02961.x.