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伴有脑膨出的综合征。

Syndromes with cephaloceles.

作者信息

Cohen M M, Lemire R J

出版信息

Teratology. 1982 Apr;25(2):161-72. doi: 10.1002/tera.1420250206.

Abstract

Encephaloceles may occur as isolated malformations or together with other anomalies making up various syndromes or associations. With the possible exception of the aberrant tissue band syndrome and the Meckel syndrome, little attention has been paid to syndromes with encephaloceles as a group. This paper discusses syndromes of known genesis, including the aberrant tissue band syndrome, Chemke syndrome, cryptophthalmos syndrome, dyssegmental dwarfism, frontonasal dysplasia, Knobloch syndrome, Meckel syndrome, pseudo-Meckel syndrome, von Voss syndrome, and warfarin syndrome. Associations include a wide range of anomalies that may occur with encephalocele. Some abnormalities are secondary to encephalocele formation; others represent primary noncontiguous embryonic malformations. Associated anomalies include absent corpus callosum, orofacial clefting, craniostenosis, Dandy-Walker defect, Arnold-Chiari defect, ectrodactyly, hemifacial microsomia, hypothalamic-pituitary dysfunction, Klippel-Feil anomaly, iniencephaly, and myelomeningocele. Finally, several other conditions with encephalocele are discussed. Some may represent true low-frequency associations; others are spurious.

摘要

脑膨出可能作为孤立的畸形出现,或与构成各种综合征或联合征的其他异常一起出现。除了异常组织带综合征和梅克尔综合征外,作为一个整体,以脑膨出为特征的综合征很少受到关注。本文讨论了已知病因的综合征,包括异常组织带综合征、切姆克综合征、隐眼综合征、节段性侏儒症、鼻额发育不良、诺布洛赫综合征、梅克尔综合征、假性梅克尔综合征、冯·沃斯综合征和华法林综合征。联合征包括可能与脑膨出同时出现的广泛异常。一些异常是脑膨出形成的继发性结果;其他异常则代表原发性非连续性胚胎畸形。相关异常包括胼胝体缺失、口面裂、颅骨狭窄、丹迪-沃克畸形、阿诺德-奇亚里畸形、缺指(趾)畸形、半侧颜面短小畸形、下丘脑-垂体功能障碍、克利佩尔-费尔畸形、枕颈露脑畸形和脊髓脊膜膨出。最后,讨论了其他几种伴有脑膨出的情况。一些可能代表真正的低频联合征;其他则是假性的。

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