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中耳炎的遗传学

The genetics of otitis media.

作者信息

Casselbrant M L, Mandel E M

机构信息

Department of Pediatric Otolaryngology, Children's Hospital of Pittsburgh, Departments of Otolaryngology and Pediatrics, University of Pittsburgh School of Medicine, 3705 Fifth Avenue, Pittsburgh, PA 15213, USA.

出版信息

Curr Allergy Asthma Rep. 2001 Jul;1(4):353-7. doi: 10.1007/s11882-001-0048-9.

Abstract

There is significant evidence from epidemiologic, anatomic, physiologic, and immunologic studies that susceptibility to recurrent episodes of acute otitis media (OM) and persistent OM with effusion is largely genetically determined. The genetics of OM are most likely complex, i.e., many genes are probably contributing to the overall phenotype. The knowledge of a hereditary component has important implications because closer surveillance of children at risk for OM could result in earlier detection and treatment. Further, once OM susceptibility genes have been identified it may be possible to develop molecular diagnostic assays that could enable the clinician to identify the child at high risk for OM and to develop more focused treatments in the future.

摘要

来自流行病学、解剖学、生理学和免疫学研究的大量证据表明,复发性急性中耳炎(OM)和持续性分泌性中耳炎易感性在很大程度上由基因决定。中耳炎的遗传学很可能很复杂,也就是说,许多基因可能对整体表型都有影响。了解遗传因素具有重要意义,因为对中耳炎高危儿童进行更密切的监测可能会实现早期检测和治疗。此外,一旦确定了中耳炎易感基因,或许就有可能开发分子诊断检测方法,使临床医生能够识别出中耳炎高危儿童,并在未来制定更有针对性的治疗方案。

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