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伴有唇腭裂的综合征

Syndromes with cleft lip and cleft palate.

作者信息

Cohen M M

出版信息

Cleft Palate J. 1978 Oct;15(4):306-28.

PMID:281275
Abstract

A series of tables is presented as a diagnostic aid for the clinician when he confronts a patient who has a cleft lip and/or palate, together with associated anomalies. The tables provide a rapid way of sorting through the recognized syndromes with orofacial clefting in search of a possible overall diagnosis. Today, 154 such syndromes are recognized. This is more than twice as many as were known in 1971. Undoubtedly, many new syndromes with orofacial clefting will be delineated in the future.

摘要

当临床医生面对患有唇裂和/或腭裂以及相关异常的患者时,会给出一系列表格作为诊断辅助工具。这些表格提供了一种快速方法,可梳理出伴有口面部裂隙的已确认综合征,以寻找可能的总体诊断。如今,已确认154种此类综合征。这比1971年已知的数量多出两倍多。毫无疑问,未来还会发现许多新的伴有口面部裂隙的综合征。

相似文献

1
Syndromes with cleft lip and cleft palate.伴有唇腭裂的综合征
Cleft Palate J. 1978 Oct;15(4):306-28.
2
Facial clefting and its syndromes.面部裂及其综合征。
Birth Defects Orig Artic Ser. 1971 Jun;7(7):3-49.
3
The epidemiology of orofacial clefts. 2. Associated malformations.口面部裂隙的流行病学。2. 相关畸形。
J Craniofac Genet Dev Biol. 1996 Oct-Dec;16(4):242-8.
4
Studies of cleft lip and cleft palate in east European populations.东欧人群唇腭裂的研究。
Prog Clin Biol Res. 1980;46:249-96.
5
Genetic considerations in clefts of the lip and palate.唇腭裂的遗传学因素
Clin Plast Surg. 1985 Oct;12(4):533-42.
6
Factors determining occurrence of cleft lip and cleft palate.决定唇腭裂发生的因素。
Surg Gynecol Obstet. 1978 Jan;146(1):105-10.
7
Prenatal diagnosis and management of orofacial clefts.口腔颌面裂的产前诊断与管理
Prenat Diagn. 2000 Feb;20(2):149-51.
8
[Cleft lip and palate: thoughts about associated anomalies].[唇腭裂:关于相关异常的思考]
Ned Tijdschr Tandheelkd. 1997 Feb;104(2):81-2.
9
Epidemiology and etiology of clefts.腭裂的流行病学与病因学
Birth Defects Orig Artic Ser. 1971 Jun;7(7):50-3.
10
A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.一种伴有后腭裂、多发颈胸椎椎体异常和髂骨发育不全的致死性、无法分类的短肢侏儒症:常染色体隐性遗传的证据
Genet Couns. 1998;9(1):61-2.

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In the Shadows of Rarity: A Case Report of Syndromic Cleft Lip and Palate!罕见病症的阴影下:一例综合征性唇腭裂病例报告!
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2
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Genes (Basel). 2023 Aug 9;14(8):1603. doi: 10.3390/genes14081603.
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Non-syndromic Cleft Palate: An Overview on Human Genetic and Environmental Risk Factors.非综合征性腭裂:人类遗传和环境风险因素概述
Front Cell Dev Biol. 2020 Oct 20;8:592271. doi: 10.3389/fcell.2020.592271. eCollection 2020.
7
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Ann Ib Postgrad Med. 2020 Jun;18(1):S16-S21.
8
Craniofacial Anomaly Association with the Internal Malformations in the Pediatric Age Group in Al-Fallujah City-Iraq.伊拉克费卢杰市儿科年龄段颅面异常与内部畸形的关联。
Biomed Res Int. 2020 Aug 18;2020:4725141. doi: 10.1155/2020/4725141. eCollection 2020.
9
Cellular and molecular mechanisms of cleft palate development.腭裂发育的细胞和分子机制。
Laryngoscope Investig Otolaryngol. 2018 Nov 15;4(1):160-164. doi: 10.1002/lio2.214. eCollection 2019 Feb.
10
Risk factors involved in orofacial cleft predisposition - review.口腔颌面部裂隙易感性相关危险因素——综述
Open Med (Wars). 2015 Feb 5;10(1):163-175. doi: 10.1515/med-2015-0027. eCollection 2015.