颅缝早闭。

Q4 Medicine

Ugeskrift for laeger Pub Date : 2025-03-17 DOI:10.61409/V06240423

Mikkel Bundgaard Skotting, Jane Skjøth-Rasmussen, Thomas Kofod, Carl Christian Larsen

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引用次数: 0

摘要

在这篇综述中，颅缝闭锁是一种以一条或多条颅缝过早融合为特征的疾病，导致颅骨发育异常。它可以作为一种非综合征性疾病发生，也可以与颅面综合征和学习困难有关。每1300 - 2500名新生儿中就有1人患有这种疾病。诊断包括临床评估和放射学确认。手术是主要的治疗方法。重要的是要区分颅缝闭锁与位置性斜头畸形，以确保适当的管理和治疗。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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[Craniosynostosis].

In this review craniosynostosis is a condition characterized by the premature fusion of one or more cranial sutures, leading to abnormal skull development. It can occur as a non-syndromal condition or be associated with craniofacial syndromes and learning difficulties. The condition affects 1 in 1.300-2.500 newborns. Diagnosis involves clinical evaluation and radiological confirmation. Surgery is the primary treatment. It is important to distinguish craniosynostosis from positional plagiocephaly to ensure appropriate management and treatment.

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来源期刊

Ugeskrift for laeger Medicine-Medicine (all)

CiteScore

0.20

自引率

0.00%

发文量

345

期刊介绍： The Ulster Medical Journal is an international general medical journal with contributions on all areas of medical and surgical specialties relevant to a general medical readership. It retains a focus on material relevant to the health of the Northern Ireland population. The Honorary Editor would welcome offers of papers for publication. Prospective authors are invited to read the notice to contributors.