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患有多种牙齿和口腔面部异常的帕皮永-勒热和普索姆综合征患者。

Papillon-Léage and psaume syndrome patient with multiple dental and orofacial anomalies.

作者信息

Kilinc D D, Ozsarp E

机构信息

Department of Orthodontics, Faculty of Dentistry, Istanbul Medipol University, Istanbul, Turkey.

出版信息

Niger J Clin Pract. 2019 Jun;22(6):872-876. doi: 10.4103/njcp.njcp_451_18.

Abstract

Papillon-Léage-Psaume Syndrome, also known as oral-facial-digital syndrome (OFDS) type I, describes a group of neurodevelopmental disorders that are characterized by anomalies of the oral cavity, facial features, and the digits. Central nervous system (CNS) anomalies and visceral organ abnormalities such as kidney, pancreas, and ovarian cysts can also be seen in these patients. Among 13 potential types, female-inherited OFDS type I is the most common and it has been reported to be lethal in males. After the identification of the genetic relation of OFDS in 2001, it is now known that, except X-linked OFDS Type I and VIII, generally all types of OFDSs are autosomal recessive. The dentist's knowledge about the syndrome can reduce the development of physical and dental anomalies by facilitating early diagnosis. This article presents a patient with Papillon-Léage-Psaume Syndrome (Oral-Facial-Digital Syndrome Type I).

摘要

帕皮永-勒热-索姆综合征,也称为I型口面指综合征(OFDS),描述了一组神经发育障碍,其特征为口腔、面部特征和手指异常。这些患者还可见中枢神经系统(CNS)异常以及内脏器官异常,如肾囊肿、胰腺囊肿和卵巢囊肿。在13种潜在类型中,女性遗传的I型OFDS最为常见,据报道该型在男性中是致命的。自2001年确定OFDS的遗传关系后,现在已知,除X连锁的I型和VIII型OFDS外,一般所有类型的OFDS都是常染色体隐性遗传。牙医对该综合征的了解有助于早期诊断,从而减少身体和牙齿异常的发生。本文介绍了一名患有帕皮永-勒热-索姆综合征(I型口面指综合征)的患者。

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