Nazer J, Hubner M E, Catalán J, Cifuentes L
Unidad de Neonatología, Maternidad Hospital Clínico de la Universidad de Chile, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile.
Rev Med Chil. 2001 Mar;129(3):285-93.
ECLAMC is a registry, aimed to assess the incidence of congenital malformations, that started in 1967 and Chile incorporated to it in 1969.
To report the incidence of cleft lip/palate, updated to 1999 in the University of Chile Maternity Hospital and other Chilean hospitals participating in the ECLAMC.
A review of the ECLAMC database that registers all births or stillbirths of more than 500 g.
The incidence of orofacial cleft, at the University of Chile Maternity Hospital, in the period 1991-1999 was 17.8 per 10,000 (12.6 for cleft lip and 5.2 for cleft palate). The incidence in the rest of participating hospitals was 12.04 and 4.6 respectively. Males had a higher incidence of cleft lip and 80% of children with cleft palate, had other malformations, most of them as part of a syndrome (13 and 18 trisomy, holoproscencephalia, Pierre Robin, Apert en EE syndromes, anencephaly etc). In three of 12 children with cleft lip but without cleft palate, there was a relative with the same malformation.
It is proposed that both entities, cleft lip with or without cleft palate and cleft palate without cleft lip, are two etiopathogenically different conditions.
ECLAMC是一个旨在评估先天性畸形发病率的登记处,始于1967年,智利于1969年加入。
报告智利大学妇产医院及其他参与ECLAMC的智利医院截至1999年唇腭裂的发病率。
回顾ECLAMC数据库,该数据库记录所有体重超过500克的活产或死产情况。
1991 - 1999年期间,智利大学妇产医院口面部裂的发病率为每10000例中有17.8例(唇裂为12.6例,腭裂为5.2例)。其他参与医院的发病率分别为12.04和4.6。男性唇裂发病率较高,80%的腭裂患儿有其他畸形,其中大多数是综合征的一部分(13三体和18三体、全前脑畸形、皮埃尔·罗宾综合征、Apert综合征、无脑儿等)。在12例仅有唇裂而无腭裂的患儿中,有3例有亲属患相同畸形。
提出唇裂伴或不伴腭裂以及单纯腭裂这两种情况在病因上是不同的。