Froster-Iskenius U G, Baird P A
Institut für Humangenetik, Medizinische Universität zu Lübeck, Federal Republic of Germany.
Teratology. 1989 Feb;39(2):127-35. doi: 10.1002/tera.1420390205.
Limb reduction defects occurring among 1,213,913 consecutive livebirths in British Columbia during the period 1952-1984 inclusive were reviewed. A total of 659 cases of limb reduction defects were identified, 393 of them involving the long bones and 190 of them more than one limb. The time period 1966-1984, during which ascertainment was consistent, was evaluated, and an incidence of 5.97 per 10,000 livebirths (1 in 1,692 live births) was found. The data were evaluated for trends over time, sex ratio, and regional and ethnic distribution. Associated anomalies of other organ systems in these cases were analyzed, and overall about one-half of the cases have additional defects. The majority of these additional defects affect the musculoskeletal system and include such entities as clubfoot, hip dislocation, and congenital contractures. Defects are also frequent in other organ systems, such as the cardiovascular, gastrointestinal, and genitourinary systems. By far the most common limb defects are terminal longitudinal defects then terminal transverse defects. Of all cases of limb defects, 75% are upper limb and 25% lower limb. We found no evidence that one side is affected more frequently. About 6.5% of cases had another family member registered with a skeletal defect; 12.9% of cases died within the first year of life, the majority (85%) of those dying having additional defects. Etiological considerations are discussed for some subgroups.(ABSTRACT TRUNCATED AT 250 WORDS)
对1952年至1984年(含)期间不列颠哥伦比亚省1,213,913例连续活产中出现的肢体减少缺陷进行了回顾。共识别出659例肢体减少缺陷病例,其中393例涉及长骨,190例涉及一个以上肢体。对1966年至1984年期间(确定情况一致)进行了评估,发现活产发病率为每10,000例中有5.97例(1/1,692活产)。对数据进行了随时间的趋势、性别比以及区域和种族分布的评估。分析了这些病例中其他器官系统的相关异常情况,总体而言,约一半的病例有其他缺陷。这些额外缺陷大多数影响肌肉骨骼系统,包括马蹄内翻足、髋关节脱位和先天性挛缩等情况。其他器官系统,如心血管、胃肠道和泌尿生殖系统中也经常出现缺陷。迄今为止,最常见的肢体缺陷是末端纵向缺陷,其次是末端横向缺陷。在所有肢体缺陷病例中,75%为上肢缺陷,25%为下肢缺陷。我们没有发现一侧受影响更频繁的证据。约6.5%的病例有另一名家庭成员登记有骨骼缺陷;12.9%的病例在出生后第一年内死亡,其中大多数(85%)死亡者有其他缺陷。对一些亚组的病因进行了讨论。(摘要截断于250字)