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三名患独眼全前脑畸形胎儿的颅面部骨骼发育情况

Cranio-facial skeletal development in three human synophthalmic holoprosencephalic fetuses.

作者信息

Arnold W H, Sperber G H, Machin G A

机构信息

Department of Anatomy II, Faculty of Dentistry, University of Witten/Herdecke, Germany.

出版信息

Ann Anat. 1998 Feb;180(1):45-53. doi: 10.1016/s0940-9602(98)80131-3.

Abstract

In three human fetuses with synophthalmic holoprosencephaly (8, 14, 23 wks. p.c.) and two normal human fetuses (9 and 13 wks. p.c.) the anatomy of the cranial base, facial cranium and their relation to the notochord was studied using serial histological sections and computer aided three-dimensional reconstruction methods. Mesethmoidal cartilage differentiation was variably deficient in all three holoprosencephalic cases. The premaxillary bones were rudimentary with missing tooth buds. The development of the sphenoid bone was defective in two of the holoprosencephalic cases (8, 14 wks. p.c.). The notochord terminated normally within the sphenoid body in all investigated cases. Our results indicate that in holoprosencephaly there is a general defect in the midline cranial cartilage differentiation rostral to the notochord.

摘要

在三个患有独眼全前脑畸形的人类胎儿(妊娠8周、14周、23周)以及两个正常人类胎儿(妊娠9周和13周)中,利用连续组织学切片和计算机辅助三维重建方法,研究了颅底、面颅骨的解剖结构及其与脊索的关系。在所有三例全前脑畸形病例中,筛骨软骨分化均存在不同程度的缺陷。上颌骨发育不全,牙蕾缺失。在两例全前脑畸形病例(妊娠8周、14周)中,蝶骨发育存在缺陷。在所有研究病例中,脊索均正常终止于蝶骨体内部。我们的结果表明,在全前脑畸形中,脊索前方的中线颅骨软骨分化普遍存在缺陷。

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