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儿童斜视不同表型形式与一个隐性易感基因座(16p13.12 - p12.3)的潜在联系。

Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3).

作者信息

Khan Arif O, Shinwari Jameela, Abu Dhaim Nada, Khalil Dania, Al Sharif Latifa, Al Tassan Nada

机构信息

Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

出版信息

Mol Vis. 2011 Apr 19;17:971-6.

Abstract

PURPOSE

To perform linkage analysis on an inbred family with members who exhibit different phenotypic forms of childhood strabismus.

METHODS

Prospective clinical examination and linkage analysis.

RESULTS

three of the ten siblings and their cousin each had a different phenotypic form of childhood strabismus: infantile esotropia with convergence excess, esotropia associated with anisometropic amblyopia, unilateral esotropic Duane syndrome, and monocular elevation deficiency. Linkage analysis for the four strabismic individuals, an unaffected sibling, and the unaffected parents identified a single disease locus on chromosome 16p13.12-p12.3 (Ensembl cytogenetic band) with a 2.5 maximum logarithm of odds score. The region is 6 MB in size and comprises 80 genes.

DISCUSSION

Linkage analysis in this unique family suggests that childhood strabismus can be recessive and that different phenotypic forms of childhood strabismus can share the same underlying genotype.

摘要

目的

对一个近亲家庭进行连锁分析,该家庭中的成员表现出不同表型形式的儿童斜视。

方法

前瞻性临床检查和连锁分析。

结果

十个兄弟姐妹中的三个及其堂兄弟/姐妹各自患有不同表型形式的儿童斜视:伴有过度集合的婴儿型内斜视、与屈光参差性弱视相关的内斜视、单侧内斜视型杜安综合征和单眼上睑下垂不足。对四名斜视个体、一名未受影响的兄弟姐妹以及未受影响的父母进行连锁分析,在16号染色体p13.12 - p12.3(Ensembl细胞遗传学带)上确定了一个单一疾病位点,最大对数优势分数为2.5。该区域大小为6兆碱基,包含80个基因。

讨论

在这个独特的家庭中进行的连锁分析表明,儿童斜视可能是隐性的,并且不同表型形式的儿童斜视可能共享相同的潜在基因型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba01/3084218/ec145d1cd3ea/mv-v17-971-f1.jpg

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