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软骨基质缺陷(CMD):小鼠中的一种新的常染色体隐性致死突变。

Cartilage matrix deficiency (cmd): a new autosomal recessive lethal mutation in the mouse.

作者信息

Rittenhouse E, Dunn L C, Cookingham J, Calo C, Spiegelman M, Dooher G B, Bennett D

出版信息

J Embryol Exp Morphol. 1978 Feb;43:71-84.

PMID:632744
Abstract

A new autosomal recessive lethal mutation in the mouse designated cartilage matrix deficiency (cmd) is described. Homozygotes are dwarfed, and have abnormally short trunk, limbs, tail and snout, as well as a protruding tongue and cleft palate. The abdomen is distended because the foreshortened rib cage and spinal column forces the liver ventrad from its normal location. Histological and electron microscopic study reveals a deficiency of cartilage matrix in tracheal cartilage and in all cartilagenous bones examined. The syndrome closely resembles the rare lethal condition achondrogenesis, found in human infants, which is also believed to be due to an autosomal recessive gene.

摘要

本文描述了一种新的小鼠常染色体隐性致死突变,称为软骨基质缺乏症(cmd)。纯合子体型矮小,躯干、四肢、尾巴和口鼻部异常短小,还有舌头突出和腭裂。腹部膨胀,因为缩短的肋骨和脊柱将肝脏从其正常位置挤向腹侧。组织学和电子显微镜研究显示,气管软骨和所有检查的软骨性骨骼中软骨基质缺乏。该综合征与人类婴儿中发现的罕见致死性疾病软骨发育不全非常相似,后者也被认为是由常染色体隐性基因引起的。

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