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人类18三体胎儿中轴骨骼的畸形模式。

Pattern of malformations in the axial skeleton in human trisomy 18 fetuses.

作者信息

Kjaer I, Keeling J W, Hansen B F

机构信息

Department of Orthodontics, School of Dentistry, University of Copenhagen, Denmark.

出版信息

Am J Med Genet. 1996 Nov 11;65(4):332-6. doi: 10.1002/(SICI)1096-8628(19961111)65:4<332::AID-AJMG16>3.0.CO;2-V.

Abstract

We examined and described the development and abnormalities of the axial skeleton in 10 human trisomy 18 fetuses. Whole-body radiographs and radiographs of midsagittal tissue blocks of the cranial base and the spine were studied. In 3 fetuses no spinal radiographs were available. Seven osseous regions or fields along the body axis were analyzed, four in the spine, and three in the cranial base and nasal bones. Malformations occurred in the occipital field in all fetuses. This was a characteristic notching, either unilateral or bilateral, of the basilar part of the occipital bone. Nasal bones were abnormal in 8 cases, either absent or hypoplastic. Malformations were found in the thoracic and/or lumbosacral field in 7 fetuses. A single abnormality was found in the cervical spine in one fetus. The pattern of axial skeletal malformation in trisomy 18 fetuses recorded in the present study has not been described previously. Axial skeletal radiography should be included in autopsies of fetuses when chromosome disorders are present or suspected. The methods applied here are unaffected by autolysis.

摘要

我们检查并描述了10例18三体胎儿中轴骨骼的发育及异常情况。研究了全身X线片以及颅底和脊柱矢状中组织块的X线片。3例胎儿没有脊柱X线片。沿着身体轴线分析了7个骨区域或部位,其中4个在脊柱,3个在颅底和鼻骨。所有胎儿的枕部区域均出现畸形。表现为枕骨基底部单侧或双侧的特征性切迹。8例鼻骨异常,表现为缺如或发育不全。7例胎儿的胸段和/或腰骶段出现畸形。1例胎儿颈椎出现单一异常。本研究记录的18三体胎儿中轴骨骼畸形模式此前尚未见报道。当存在或怀疑有染色体疾病时,胎儿尸检应包括中轴骨骼X线检查。此处应用的方法不受自溶影响。

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