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130例腭心面综合征患者的临床特征。鲁汶的经验。

Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.

作者信息

Vantrappen G, Rommel N, Devriendt K, Cremers C W, Feenstra L, Fryns J P

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Leuven.

出版信息

Acta Otorhinolaryngol Belg. 2001;55(1):43-8.

Abstract

The velo-cardio-facial syndrome (VCFS) is a leading cause of velopharyngeal dysfunction and cleft palate and caused by a submicroscopic deletion in the long arm of chromosome 22 (band 22q11). During the last 5 years, 130 patients with a 22q11 deletion were diagnosed in Leuven. Most patients presented a wide variety of the classical features of the velo-cardio-facial syndrome. Velopharyngeal dysfunction was almost always present whereas an isolated cleft lip/palate was observed in a minority of patients. The velopharyngeal function can be evaluated by the classic combination of indirect and direct techniques. Because of the frequent occurrence of the velo-cardio-facial syndrome, estimated at around 1/4000 live births, and given the extremely broad clinical spectrum which makes clinical diagnosis difficult, screening of patients with velopharyngeal dysfunction for a deletion 22q11 is indicated.

摘要

腭心面综合征(VCFS)是腭咽功能障碍和腭裂的主要病因,由22号染色体长臂(22q11带)的亚显微缺失引起。在过去5年中,鲁汶诊断出130例22q11缺失患者。大多数患者表现出腭心面综合征的多种典型特征。几乎总是存在腭咽功能障碍,而少数患者观察到孤立性唇腭裂。腭咽功能可通过间接和直接技术的经典组合进行评估。由于腭心面综合征的发病率较高,估计约为1/4000活产,且临床谱极广,导致临床诊断困难,因此建议对腭咽功能障碍患者进行22q11缺失筛查。

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