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Identification and Treatment of Congenital Muscular Torticollis in Infants

机译:婴儿先天性肌性斜颈的鉴定与治疗

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Torticollis is a clinical sign or symptom that could be the result of a variety of underlying disorders. Congenital muscular torticollis (CMT) is a postural deformity detected at birth or shortly after birth, primarily resulting from unilateral shortening and fibrosis of the sternocleidomastoid muscle (SCM). Infants with CMT display head tilt to one side, which is often combined with rotation of the head to the opposite side (Figure I). CMT is estimated to occur in one infant of every 300 live births. Plagiocephaly is reported as a coexisting impairment in 80% to 90.1% of children with CMT.The purposes of this report are to provide an overview of the CMT literature with attention to the relationship between torticollis and plagiocephaly and to describe current management of infants with congenital muscular torticollis with or without plagiocephaly.
机译:斜颈是一种临床症状或体征,可能是多种潜在疾病的结果。先天性肌斜颈(CMT)是在出生时或出生后不久就检测到的姿势畸形,主要是由于胸锁乳突肌(SCM)的单侧缩短和纤维化引起的。带有CMT的婴儿显示头向一侧倾斜,这通常与头部向相反侧的旋转结合在一起(图I)。据估计,每300名活产婴儿中就有一名发生CMT。据报道,80%至90.1%的CMT儿童合并有头颅畸形。本报告的目的是概述CMT文献,关注斜颈与斜头畸形之间的关系,并描述当前对先天性婴儿的管理肌肉斜颈伴或不伴斜头畸形。

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