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首页> 外文期刊>The Journal of clinical pediatric dentistry >Prevalence and characteristics of non-syndromic orofacial clefts and the influence of consanguinity
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Prevalence and characteristics of non-syndromic orofacial clefts and the influence of consanguinity

机译:非综合征性口面部裂隙的患病率和特征以及血缘的影响

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The Objective of this study was to identify the prevalence and describe the characteristics of non-syndromic orofacial cleft (NSOFC) in Jeddah, Saudi Arabia and examine the influence of consanguinity. Study Design: Six hospitals were selected to represent Jeddah's five municipal districts. New born infants with NSOFC born between 1st of January 2010 to 31st of December 2011 were clinically examined and their number compared to the total number of infants born in these hospitals to calculate the prevalence of NSOFC types and sub-phenotypes. Referred Infants were included for the purpose of studying NSOFC characteristics and their relationship to consanguinity. Information on NSOFC infants was gathered through parents' interviews, infants' files and patient examinations. Results: Prospective surveillance of births resulted in identifying 37 NSOFC infants born between 1st of January 2010 to 31st of December 2011 giving a birth prevalence of 0.80/1000 living births. The total infants seen, including referred cases, were 79 children. Consanguinity among parents of cleft palate (CP) cases was statistically higher than that among cleft lip with or without cleft palate (CL/P) patients (P=0.039). Although there appears to be a trend in the relationship between consanguinity and severity of CL/P sub-phenotype, it was not statistically significant (P= 0.248). Conclusions: Birth prevalence of NSOFC in Jeddah City was 0.8/1000 live births with CL/P: 0.68/1000 and CP: 0.13/1000. Both figures were low compared to the global birth prevalence (NSOFC: 1.25/1000, CL/P: 0.94/1000 and CP: 0.31/1000 live births). Consanguineous parents were statistically higher among CP cases than among other NSOFC phenotypes.
机译:这项研究的目的是确定沙特阿拉伯吉达的患病率并描述非综合征性口面部裂隙(NSOFC)的特征,并研究血缘的影响。研究设计:选择了六家医院代表吉达的五个市政区。对2010年1月1日至2011年12月31日之间出生的NSOFC新生儿进行临床检查,并将其数量与这些医院出生的婴儿总数进行比较,以计算NSOFC类型和亚表型的患病率。为了研究NSOFC的特征及其与血缘关系,纳入了推荐婴儿。有关NSOFC婴儿的信息是通过父母的访谈,婴儿档案和患者检查收集的。结果:对出生进行的前瞻性监测确定了在2010年1月1日至2011年12月31日之间出生的37名NSOFC婴儿,其出生率为0.80 / 1000个活产婴儿。包括转诊病例在内的婴儿总数为79名儿童。 c裂(CP)病例的父母之间的血缘关系在统计学上高于有或没有c裂(CL / P)的唇裂患者(P = 0.039)。尽管血缘和CL / P亚型的严重程度之间存在关系的趋势,但在统计学上无统计学意义(P = 0.248)。结论:吉达市NSOFC的出生率为0.8 / 1000活产,CL / P:0.68 / 1000,CP:0.13 / 1000。与全球出生率相比,这两个数字均较低(NSOFC:1.25 / 1000,CL / P:0.94 / 1000,CP:0.31 / 1000活产)。在CP病例中,近亲父母比其他NSOFC表型在统计学上更高。

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