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不明原因的眼裂缺损的表型相关性。

Phenotypic correlations of ocular coloboma without known cause.

作者信息

Leppig K A, Pagon R A

机构信息

Department of Medicine, University of Washington School of Medicine, Seattle 98195.

出版信息

Clin Dysmorphol. 1993 Oct;2(4):322-31.

PMID:8305963
Abstract

Ocular coloboma can occur as an autosomal dominant condition or as part of a known syndrome or chromosomal abnormality. We have designated those patients with ocular coloboma who do not fit into any of these three groups as having coloboma without known cause. We completed a retrospective review of 58 patients from our clinics with coloboma without known cause to determine the frequency of other co-existing congenital malformations and mental retardation. Mental retardation was present in 14 of the 42 patients (33%) who were more than 1 year of age. However, only 14% of the children who had no other malformations had mental retardation, whereas 57% of those with other malformations were mentally retarded. We found that the severity of the colobomatous malformation did not correlate with intellect.

摘要

眼裂缺损可作为常染色体显性疾病出现,或作为已知综合征或染色体异常的一部分出现。我们将那些不符合这三组中任何一组的眼裂缺损患者定义为病因不明的眼裂缺损。我们对来自我们诊所的58例病因不明的眼裂缺损患者进行了回顾性研究,以确定其他并存的先天性畸形和智力发育迟缓的发生率。在42例年龄超过1岁的患者中,有14例(33%)存在智力发育迟缓。然而,在没有其他畸形的儿童中,只有14%存在智力发育迟缓,而在有其他畸形的儿童中,这一比例为57%。我们发现眼裂缺损畸形的严重程度与智力无关。

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