Evidence map›Paper›PMID 27385965›Full record

ArticleMolecular syndromology2016

Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract.

Olga Messina-Baas, Manuel L Gonzalez-Garay, Luz M González-Huerta, Jaime Toral-López, Sergio A Cuevas-Covarrubias

Open access · bronzeAbstract read
In one paragraph

Article in Molecular syndromology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 2 countries.

Olga Messina-BaasDepartments of Ophthalmology, Hospital General de México, Facultad de Medicina, UNAM, Mexico City, Mexico.
Manuel L Gonzalez-GarayDivision of Next Generation Sequencing, Center for Molecular Imaging, The Brown Foundation Institute of Molecular Medicine, University of Texas, Houston, Tex., USA.
Luz M González-HuertaDepartments of Medical Genetics, Hospital General de México, Facultad de Medicina, UNAM, Mexico City, Mexico.
Jaime Toral-LópezDepartment of Medical Genetics, Centro Medico, ISSEMyM, Ecatepec de Morelos, Mexico.
Sergio A Cuevas-CovarrubiasDepartment of Medical Genetics, Centro Medico, ISSEMyM, Ecatepec de Morelos, Mexico.
Universidad de Ecatepec · MXBrown Foundation · USHospital General de México · MXOphthalmology Associates (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital cataract, an important cause of reversible blindness, is due to several causes including Mendelian inheritance. Thirty percent of cataracts are hereditary with participation of the gamma crystallin genes. Clinical and genetic heterogeneity is observed in patients with gene mutations and congenital cataract; about 40 genetic loci have been associated with hereditary cataract. In this study, we identified the underlying genetic cause of an autosomal dominant pulverulent cataract (ADPC) in a large Mexican family. Twenty-one affected patients and 20 healthy members of a family with ADPC were included. Genomic DNA was analyzed by whole exome sequencing in the proband, a normal daughter, and in an affected son, whereas DNA Sanger sequencing was performed in all members of the family. After the bioinformatics analysis, all samples were genotyped using Sanger sequencing to eliminate variants that do not cosegregate with the cataract. We observed a perfect cosegregation of a nonsense mutation c.475C>T (p.Q155*) in exon 6 of the CRYBB2 gene with ADPC. We calculated a logarithm of the odds score of 5.5. This mutation was not detected in healthy members of the family and in 100 normal controls. This is the first Mexican family with ADPC associated with a p.Q155* mutation. Interestingly, this specific mutation in the CRYBB2 gene seems to be exclusively associated with pulverulent/cerulean cataract (with some clinical variability) independent of the population's genetic background.

Indexed as

Autosomal dominant pulverulent cataractClinical heterogeneityCRYBB2CRYBB2P1Whole exome sequencing

Identifiers

PMID27385965
PMCPMC4906430
OpenAlexW2341144788

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.