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下肢发育不全的流行病学、病因学及遗传学方面

Epidemiology, etiology, and genetic aspects of reduction deficiencies of the lower limb.

作者信息

Ghanem Ismat

机构信息

Pediatric Orthopaedic Surgery, Hôtel-Dieu de France Hospital, Saint Joseph University, Achrafieh, Beirut, Lebanon,

出版信息

J Child Orthop. 2008 Oct;2(5):329-32. doi: 10.1007/s11832-008-0098-9. Epub 2008 Apr 9.

Abstract

Although the majority of lower limb deficiencies are of sporadic occurrence and of unknown etiology, genetic factors are involved in a significant number, with variable modes of inheritance. A better-informed public is demanding advice concerning cause and recurrence. Careful scrutiny of the medical history and family tree and attention to phenotypic details may help to delineate entities. At times, specific chromosomal tests are important, mainly when there is bilateral or multiorgan involvement or when limb deficiency is associated with developmental delay and/or mental retardation. This paper is intended to refamiliarize the orthopaedic community with basic genetic aspects regulating reduction deficiencies of the lower limbs, and to emphasize on the importance and indications of genetic counseling.

摘要

虽然大多数下肢缺陷是散发性的且病因不明,但相当一部分涉及遗传因素,遗传方式各不相同。知识日益丰富的公众要求得到有关病因和复发情况的建议。仔细审查病史和家族谱系并关注表型细节可能有助于明确诊断。有时,特定的染色体检查很重要,主要是在出现双侧或多器官受累,或肢体缺陷与发育迟缓及/或智力迟钝相关时。本文旨在使骨科界重新熟悉调节下肢肢体缺损的基本遗传学知识,并强调遗传咨询的重要性和适应证。

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