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母体给予三嗪后小鼠胚胎的耳部畸形及其临床意义。

Ear malformations in the mouse embryo following maternal administration of triazene, with clinical implications.

作者信息

Louryan S, Heymans O, Goffard J C

机构信息

Laboratoire d'Anatomie et Embryologie Humaines, Faculté de Médecine (C.P. 619), Université Libre de Bruxelles, Belgium.

出版信息

Surg Radiol Anat. 1995;17(1):59-63. doi: 10.1007/BF01629502.

DOI:10.1007/BF01629502
PMID:7597567
Abstract

Triazene administration to 10-day pregnant mice gave rise to severe ear abnormalities, including middle ear ossicle malformations. The head of the malleus and the body of the incus were sometimes absent. In some instances, the stapes appeared dysplastic. The stapedial artery was often quite dilated, as well as other cephalic vessels, but qualitatively normal. Severe inner ear abnormalities were observed, as well as auditory nerve disruption, which was associated with central nervous system lesions. Multiple haematomas were present in the embryonic face, but ear abnormalities occurred even in the absence of local hemorrhages. We postulate a direct effect of the teratogen on the branchial mesenchyme. This model seems to be useful for the comprehension of human middle ear abnormalities, but does not constitute a phenocopy of hemicranial microscomia.

摘要

给怀孕10天的小鼠施用三氮烯会导致严重的耳部异常,包括中耳听小骨畸形。锤骨头部和砧骨体有时缺失。在某些情况下,镫骨发育异常。镫骨动脉以及其他头部血管常常明显扩张,但性质正常。观察到严重的内耳异常以及听神经中断,这与中枢神经系统损伤有关。胚胎面部出现多处血肿,但即使没有局部出血也会发生耳部异常。我们推测致畸剂对鳃间充质有直接作用。该模型似乎有助于理解人类中耳异常,但并不构成半侧颅面微小畸形的拟表型。

相似文献

1
Ear malformations in the mouse embryo following maternal administration of triazene, with clinical implications.母体给予三嗪后小鼠胚胎的耳部畸形及其临床意义。
Surg Radiol Anat. 1995;17(1):59-63. doi: 10.1007/BF01629502.
2
Middle ear anomalies induced by hypertriazene administration in the mouse.
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Congenital malformations of the external, middle, and inner ear produced by isotretinoin exposure in mouse embryos.小鼠胚胎暴露于异维甲酸所产生的外耳、中耳和内耳先天性畸形。
Otolaryngol Head Neck Surg. 1990 Apr;102(4):391-401. doi: 10.1177/019459989010200414.
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[Clinical aspects on chemically produced malformations in animals].[动物化学诱导畸形的临床方面]
Arch Klin Exp Ohren Nasen Kehlkopfheilkd. 1968 May 9;190(3):330-50.
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Teratology. 1987 Feb;35(1):9-18. doi: 10.1002/tera.1420350103.
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Induced and genetic mouse middle ear ossicular malformations: a model for human malformative ossicular diseases and a tool for clarifying their normal ontogenesis.诱导性和遗传性小鼠中耳听小骨畸形:人类畸形性听骨疾病的模型及阐明其正常个体发生的工具。
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Congenital perilymphatic fistula and associated middle ear abnormalities.先天性外淋巴瘘及相关中耳异常。
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本文引用的文献

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Pathogenesis of median facial clefts in mice treated with methotrexate.
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Mandibulofacial dysostosis (Treacher Collins syndrome): a new proposal for its pathogenesis.下颌面骨发育不全(特雷彻·柯林斯综合征):关于其发病机制的新观点
Am J Med Genet. 1987 Jun;27(2):359-72. doi: 10.1002/ajmg.1320270214.
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Teratogens and craniofacial malformations: relationships to cell death.致畸剂与颅面畸形:与细胞死亡的关系
Development. 1988;103 Suppl:213-31. doi: 10.1242/dev.103.Supplement.213.
9
Induced and genetic mouse middle ear ossicular malformations: a model for human malformative ossicular diseases and a tool for clarifying their normal ontogenesis.诱导性和遗传性小鼠中耳听小骨畸形:人类畸形性听骨疾病的模型及阐明其正常个体发生的工具。
Surg Radiol Anat. 1992;14(3):227-32. doi: 10.1007/BF01794945.
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