交流障碍患者颅缝闭锁的临床实践及对家庭的影响

A. M. Peters, Lindsey E. Jorgensen
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引用次数: 0

摘要

颅缝闭闭是一种先天性颅骨缝合线畸形,在儿童时期过早融合,导致颅骨不能适当扩张。这种融合的认知和身体后果会持续一生。颅缝闭锁有几种类型,这取决于缝合融合的方式,这些都有各种各样的长期后果。诊断通常是在出生后做出的,如果手术迅速完成,一些后遗症可以附加。出生时患有颅缝闭合症的孩子会有长期的并发症,鉴于她的家庭关系,作者彼得斯女士很容易意识到这一点。与患有这种疾病的人一起工作是具有挑战性的,但也是有益的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review of Craniosynostosis in Communication Disorders Practice and its Effect on my Family
Craniosynostosis is a congenital malformation of the sutures of the scull which fuse too early in childhood which does not allow the scull to expand appropriately. The cognitive and physical consequences of this fusion can last a lifetime. There are several types of craniosynostosis depending on what suture fuses and these have a variety of long-term consequences. The diagnosis is typically made after birth and some of the sequela can be appended if surgery is completed in a quick manner. The children born with craniosynostosis will have long-term complications of which the author, Ms. Peters, is readily aware given her family connection. Working with someone with this disorder can be challenging, but rewarding.
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