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首页> 外文期刊>Bosnian Journal of Basic Medical Sciences >Craniosynostosis - Recognition, clinical characteristics, and treatment
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Craniosynostosis - Recognition, clinical characteristics, and treatment

机译:颅骨前突-认识,临床特征和治疗

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摘要

Craniosynostosis is a developmental craniofacial anomaly, resulting in impairment of brain development and abnormally shaped skull. The main cause of craniosynostosis is premature closure of one or more cranial sutures. It usually occurs as an isolated condition, but may also be associated with other malformations as part of complex syndromes. When left untreated, craniosynostosis can cause serious complications, such as developmental delay, facial abnormality, sensory, respiratory and neurological dysfunction, anomalies affecting the eye, and psychological disturbances. Thus, early diagnosis, expert surgical techniques, postoperative care, and adequate follow-up are of vital importance in treating craniosynostosis.
机译:颅骨前突是颅面发育异常,导致大脑发育受损和颅骨形状异常。颅骨融合症的主要原因是过早闭合一种或多种颅骨缝线。它通常以孤立的情况发生,但也可能与其他畸形相关,作为复杂综合症的一部分。如果不加以治疗,颅骨融合症会引起严重的并发症,例如发育延迟,面部异常,感觉,呼吸和神经功能障碍,影响眼睛的异常以及心理障碍。因此,早期诊断,专业的手术技术,术后护理和充分的随访对治疗颅骨融合症至关重要。

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