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Anterior plagiocephaly: Epidemiology, clinical findings,diagnosis, and classification. A review

机译:前头:流行病学,临床发现,诊断和分类。回顾

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Introduction: Anterior plagiocephaly due to the early unilateral fusion of the coronal suture is associated to a clinical phenotype characterized by the unilateral flattening of the frontal bone and the orbit and by the distortion and maldevelopment of adjacent cranial and facial bones. Homolateral anterior displacement of the ear and contralateral deviation of the nasal pyramid and mandible are other prominent clinical features. The differential diagnosis includes a variety of conditions characterized by facial asymmetry, namely, due to muscular alterations, anomalies of the visual function, congenital anomalies of the cervical spine and craniovertebral junction, abnormal pregnancy, and birth injuries. Anterior plagiocephaly is the direct cause of oculomotor anomalies, with a characteristic strabismus, and of progressive asymmetrical maldevelopment of the face, craniovertebral junction, and cervical spine. Methods: The medical literature was reviewed in regard to the epidemiology, clinical features, and radiological findings. Different categorization of the affected infants in specific subtypes according to the severity of the condition was analyzed. The aim was to contribute to a practical clinical classification to be utilized for the surgical indication and for predicting the prognosis according to the severity of the condition at presentation. Conclusions: Anterior plagiocephaly represents the most challenging simple suture craniosynostosis. The clinical differential diagnosis with other forms of cranial asymmetry is possible on the grounds of mere clinical findings. A classification system is necessary not only for the establishment of surgical planning but also to predict the late cosmetic and functional outcomes.
机译:简介:由于冠状缝线的早期单侧融合而导致的前斜视与临床表型有关,其特征是额骨和眼眶的单侧变平以及相邻颅骨和面骨的畸变和发育不良。耳朵的同侧前移,鼻锥和下颌骨的对侧偏斜是其他突出的临床特征。鉴别诊断包括以面部不对称为特征的多种情况,即由于肌肉改变,视觉功能异常,颈椎和颅骨交界处的先天性异常,异常妊娠和出生受伤。前斜脑畸形是动眼畸形的直接原因,其特征是斜视,并导致面部,颅椎交界处和颈椎的进行性不对称发育不良。方法:对医学文献进行了流行病学,临床特征和影像学检查的回顾。根据病情的严重性,对特定亚型的患儿进行了不同的分类。目的是根据临床表现的严重程度,为临床适应症和预测预后做出贡献。结论:前斜cephal是最具挑战性的简单缝线颅突融合术。仅凭临床发现就可能与其他形式的颅骨不对称一起进行临床鉴别诊断。分类系统不仅对于建立手术计划是必要的,而且对于预测晚期美容和功能结局也是必要的。

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