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患有皮埃尔·罗宾序列征和单纯腭裂儿童的生长情况。

Growth in children with Pierre Robin sequence and isolated cleft palate.

作者信息

Laitinen S, Heliövaara A, Pere A, Ranta R

机构信息

Department of Pedodontics and Orthodontics, University of Helsinki, Children's Hospital, Finland.

出版信息

Acta Paediatr. 1994 Nov;83(11):1161-4. doi: 10.1111/j.1651-2227.1994.tb18273.x.

Abstract

Postnatal height and weight growth were assessed in 50 children (20 boys) with Pierre Robin sequence and in 58 children (27 boys) with isolated cleft palate, born in 1967-86. The height and weight measurements from birth to 12 years were collected retrospectively from child health centers and schools. The current Finnish relative weight and SD scores for height were used for growth assessment. The birth size of children with Pierre Robin sequence did not differ from those with isolated cleft palate or from healthy children, on the basis of Finnish norms. During the first year after birth, children with Pierre Robin sequence were shorter and lighter than those with isolated cleft palate but later caught up with them and the Finnish norms. Children with Pierre Robin sequence born prematurely or with associated anomalies showed more deficient growth.

摘要

对1967年至1986年间出生的50名患有皮埃尔·罗宾序列征的儿童(20名男孩)和58名患有单纯腭裂的儿童(27名男孩)进行了出生后身高和体重增长评估。从儿童健康中心和学校回顾性收集了这些儿童从出生到12岁的身高和体重测量数据。使用芬兰当前的相对体重和身高标准差评分进行生长评估。根据芬兰的标准,患有皮埃尔·罗宾序列征的儿童出生时的大小与患有单纯腭裂的儿童或健康儿童没有差异。在出生后的第一年,患有皮埃尔·罗宾序列征的儿童比患有单纯腭裂的儿童更矮、更轻,但后来赶上了他们以及芬兰的标准。早产或伴有相关异常的患有皮埃尔·罗宾序列征的儿童生长更为不足。

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