Next-generation sequencing reveals a new mutation in the LTBP2 gene associated with microspherophakia in a Spanish family


Por: Alias, L, Crespi, J, Gonzalez-Quereda, L, Tellez, J, Martinez, E, Bernal, S, Gallano, MP

Publicada: 11 may 2018
Resumen:
Background: Microspherophakia is a rare autosomal recessive eye disorder characterized by small spherical lens. It may present as an isolated finding or in association with other ocular and/or systemic disorders. This clinical and genetic heterogeneity requires the study of large genes (ADAMTSL4, FBN1, LTBP2, ADAMTSL-10 and ADAMTSL17). The purpose of the present study is to identify the genetic cause of this pathology in a consanguineous Spanish family. Methods: A clinical exome sequencing experiment was executed by the TruSight One (R) Sequencing Panel (TSO) from lllmina(C). Sanger sequencing was used to validate the NGS results. Results: Only the insertion of an adenine in exon 36 of the LTBP2 gene (c.5439_5440insA) was associated with pathogenicity. This new mutation was validated by Sanger sequencing and segregation analysis was also performed. Haplotype analyses using the polymorphic markers D1451025, D14S43 and D14S999 dose to the LTBP2 gene indicated identity by descent in this family. Conclusion: We describe the first case of a microspherophakia phenotype associated with a novel homozygous mutation in the LTBP2 gene in a consanguineous Caucasian family by means of NGS technology.

Filiaciones:
Alias, L:
 Hosp Santa Creu & Sant Pau, Dept Genet, Pare Claret 167, Barcelona 08025, Spain

 CIBERER U705, Barcelona, Spain

Crespi, J:
 Hosp Santa Creu & Sant Pau, Dept Ophthalmol, Barcelona, Spain

Gonzalez-Quereda, L:
 Hosp Santa Creu & Sant Pau, Dept Genet, Pare Claret 167, Barcelona 08025, Spain

 CIBERER U705, Barcelona, Spain

Tellez, J:
 Hosp Santa Creu & Sant Pau, Dept Ophthalmol, Barcelona, Spain

Martinez, E:
 Hosp Santa Creu & Sant Pau, Dept Genet, Pare Claret 167, Barcelona 08025, Spain

Bernal, S:
 Hosp Santa Creu & Sant Pau, Dept Genet, Pare Claret 167, Barcelona 08025, Spain

Gallano, MP:
 Hosp Santa Creu & Sant Pau, Dept Genet, Pare Claret 167, Barcelona 08025, Spain

 CIBERER U705, Barcelona, Spain
ISSN: 14712350





BMC Medical Genetics
Editorial
BIOMED CENTRAL LTD, 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 19 Número:
Páginas:
WOS Id: 000432355600003
ID de PubMed: 29751740
imagen Gold, Green Published

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