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Achondrogenesis type II (Langer-Saldino achondrogenesis): a case report.

机译:II型手足口病(Langer-Saldino手足口病):一例病例报告。

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摘要

Achondrogenesis is a lethal form of congenital chondrodystrophy characterized by extreme micromelia. We describe a case of achondrogenesis type II (Langer-Saldino achondrogenesis) detected by prenatal ultrasonography at 20-week gestation. A dwarfed fetus with large head, short neck and chest, prominent abdomen and short limbs was terminated transvaginally. Radiologic and histopathologic examination revealed features of mild form of achondrogenesis type II. Although the case had no known risk factor and the phenotypic abnormality was mild, modern development in prenatal screening made the early detection possible.
机译:软骨形成是一种致命的先天性软骨营养不良的形式,其特征是极端的小mel。我们描述了一种在妊娠20周时通过产前超声检查发现的II型软骨发育不全(朗格-萨尔迪诺软骨发育不全)的情况。矮小的胎儿头部,颈部和胸部短,腹部突出和四肢短,经阴道终止。放射学和组织病理学检查显示II型软骨发育不良的特征。尽管该病例没有已知的危险因素,且表型异常轻微,但产前筛查的现代发展使早期发现成为可能。

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