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The profile of major congenital abnormalities in the United Arab Emirates (UAE) population.

机译:阿拉伯联合酋长国(UAE)人口中主要的先天性异常的概况。

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摘要

The aim of this study was to establish the profile of major congenital malformations in the United Arab Emirates (UAE) population which has a high rate of consanguinity. All births with birth weight above 500 g in the three hospitals in the Al Ain Medical District of UAE were prospectively studied from January 1992 to January 1994. About 98% of the births in the district occur in these three hospitals. Detailed family history and clinical and relevant laboratory investigations were recorded in each case. Necropsy was not permitted. The major malformations were classified as multiple or isolated single system abnormalities as well as genetic or non-genetic disorders. Of the 16,419 births which occurred during the two year period, 173 (10.5/1000 births) had major malformations, 90 (52%) had multiple malformations, and 83 (47.97%) had involvement of a single system. Of the infants with multiple malformations, 43 had recognised syndromes, most of which are autosomal recessive disorders with a high frequency of rare syndromes. Twenty eight (31%) had chromosomal abnormalities. The most common systems involved in infants with isolated single system malformations include gastrointestinal (33), central nervous system (17), and cardiovascular (10). While the consanguinity rate was similar (57% v 54%), the frequency of first cousin marriages was much higher (51% v 30%) in the study group compared with the figures for the general population. The consanguinity rate was highest among the syndrome cases, and related parents were more likely to have infants with multiple malformations than an isolated single system abnormality with a relative risk of 1.69 (95% CL 1.27-2.24). Genetic factors could be implicated in 116 (67%) of the 173 cases of major malformations and 49 (28%) were potentially preventable. The study suggests that genetic disorders account for a significant proportion of congenital malformation in the UAE and, thus, a genetic service should be provided as part of the preventive cae programme.
机译:这项研究的目的是确定高血缘率的阿拉伯联合酋长国(UAE)人口中主要先天畸形的概况。从1992年1月至1994年1月,对阿联酋Al Ain医疗区的三家医院中所有出生体重超过500 g的婴儿进行了前瞻性研究。该地区约98%的婴儿出生在这三家医院中。每例都记录了详细的家族史以及临床和相关的实验室检查。尸检是不允许的。主要畸形归类为多发或孤立的单系统异常以及遗传性或非遗传性疾病。在两年期间发生的16,419例出生中,有173例(10.5 / 1000例)患有严重畸形,其中90例(52%)患有多种畸形,而83例(47.97%)涉及单个系统。在具有多种畸形的婴儿中,有43个已识别出综合征,其中大多数是常染色体隐性遗传疾病,罕见综合征的发生频率很高。二十八(31%)人有染色体异常。患有孤立的单个系统畸形的婴儿所涉及的最常见系统包括胃肠道(33),中枢神经系统(17)和心血管(10)。虽然血缘关系相似(57%vs 54%),但与普通人群的数字相比,研究组的表亲结婚频率要高得多(51%vs 30%)。在综合征病例中,血缘亲缘关系发生率最高,相关父母比单独的单系统异常患多发畸形婴儿的可能性更高,相对风险为1.69(95%CL 1.27-2.24)。 173例严重畸形病例中有116例(67%)可能涉及遗传因素,而潜在的49例(28%)是可以预防的。该研究表明,遗传性疾病占阿联酋先天性畸形的很大比例,因此,作为预防性cae计划的一部分,应提供遗传服务。

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