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无虹膜、晶状体异位、上颌切牙异常与智力发育迟缓——一种常染色体隐性综合征。

Aniridia, ectopia lentis, abnormal upper incisors and mental retardation--an autosomal recessive syndrome.

作者信息

Zamzam A M, Sheriff S M, Phillips C I

机构信息

Department of Ophthalmology, Ibn Sina Hospital, Kuwait.

出版信息

Jpn J Ophthalmol. 1988;32(4):375-8.

PMID:3266265
Abstract

A 13-year-old boy presented with bilateral aniridia, ectopia lentis, two palatally placed upper incisors which may be supernumerary teeth or may be malpositioned lateral incisors, and mental retardation. The cause is very probably a single autosomal recessive gene defect although the mental state may have a separate, genetic cause. Since his parents, who are normal, are second cousins and his father's and his mother's parents are also full cousins, the coefficient of inbreeding is 1/64 which is only 25% of the coefficient for full cousinhood of parents alone (1/16). No biochemical correlate has been identified.

摘要

一名13岁男孩出现双侧无虹膜、晶状体异位、两颗位于腭侧的上颌切牙,这两颗牙可能是多生牙,也可能是错位的侧切牙,以及智力发育迟缓。病因很可能是单个常染色体隐性基因缺陷,尽管精神状态可能有独立的遗传病因。由于他的父母正常,是二级表亲,且他父亲和母亲的父母也是亲表亲,近亲系数为1/64,仅为父母均为亲表亲时近亲系数(1/16)的25%。尚未确定生化关联。

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