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[早期人类胎儿中的并眼畸形]

[Synophthalmia in an early human fetus].

作者信息

Rohrbach J M, Kendziorra H, Hungerland E

机构信息

Abteilung I (Allgemeine Augenheilkunde mit Poliklinik), Universitäts-Augenklinik.

出版信息

Klin Monbl Augenheilkd. 1999 Mar;214(3):188-92. doi: 10.1055/s-2008-1034775.

Abstract

BACKGROUND

The great majority of reports dealing with human cyclopia and synophthalmia are derived from fetuses at the end of pregnancy. Thus, data concerning early organization of the ocular anlage in this impressive ocular developmental anomaly are almost completely lacking. We therefore present a 12 week-old synophthalmic fetus.

CASE REPORT

After uneventful pregnancy spontaneous abortion occurred. Within the face of the hypotrophic fetus there was a central pigmented ocular anlage with an inferior fissure. A nose (proboscis) was not discernible. Histologically, there were two vesicles caudally which fused to one vesicle cranially. Differentiation was more advanced in the anterior and temporal parts of the anlagen. A coherent inner layer (of the optic cup) was not developed. Trisomy 13 was suspected but could not be proved by FISH-technique.

CONCLUSIONS

The fetus demonstrates that fusion of the ocular anlagen is finished at the end of the third gestational month and that synophthalmia/cyclopia is very likely to be associated with maldevelopment of the optic cup. As far as we know there is evidence for the first time that organization of the anlagen improves not only in the posterior to anterior and in the medial to lateral but also in the cranial to caudal direction.

摘要

背景

绝大多数关于人类独眼畸形和并眼畸形的报告来自妊娠末期的胎儿。因此,在这种令人印象深刻的眼部发育异常中,几乎完全缺乏有关眼原基早期组织的数据。因此,我们展示一个12周大的并眼畸形胎儿。

病例报告

妊娠过程顺利,后发生自然流产。在发育不全的胎儿面部有一个中央色素沉着的眼原基,有一条下裂。未发现鼻子(象鼻)。组织学上,尾部有两个囊泡,在头部融合为一个囊泡。眼原基的前部和颞部的分化更明显。(视杯的)连贯内层未发育。怀疑有13三体综合征,但无法通过荧光原位杂交技术证实。

结论

该胎儿表明眼原基的融合在妊娠第三个月末完成,并且并眼畸形/独眼畸形很可能与视杯发育不良有关。据我们所知,首次有证据表明眼原基的组织不仅从后向前、从内侧向外侧改善,而且从头部向尾部改善。

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