Report of a novel mutation in the slc26a2 gene found in a colombian adult patient with diastrophic dysplasia
Diastrophic Dysplasia is an osteochondrodysplasia belonging to the group of dysplasias caused by mutations in the diastrophic dysplasia sulfate transporter.Thissyndromeis amicromelic dysplasia with multiplebone deformities of the hands, feet, knees and spine. Inthis paper we report a Colombian adult...
- Autores:
-
Pineda, Tatiana
Rossi, Antonio
Bonafe, Luisa
Superti-Furga, Andrea
Velasco Parra, Harvy Mauricio
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2013
- Institución:
- Universidad Nacional de Colombia
- Repositorio:
- Universidad Nacional de Colombia
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unal.edu.co:unal/72253
- Acceso en línea:
- https://repositorio.unal.edu.co/handle/unal/72253
http://bdigital.unal.edu.co/36726/
- Palabra clave:
- Diastrophic Dysplasia
Colombian patient
Ser157Thr substitution
SLC26A2 gene
- Rights
- openAccess
- License
- Atribución-NoComercial 4.0 Internacional
| Summary: | Diastrophic Dysplasia is an osteochondrodysplasia belonging to the group of dysplasias caused by mutations in the diastrophic dysplasia sulfate transporter.Thissyndromeis amicromelic dysplasia with multiplebone deformities of the hands, feet, knees and spine. Inthis paper we report a Colombian adult patient with diastrophic dysplasia whose clinical diagnosis was confirmed at the molecular level. In this first report of diastrophic dysplasia in Colombia we found that the patient was compound heterozygote for the already reported Arg279Trp substitution and an unpublished mutation, a Ser157Thr substitution in the SLC26A2 gene. Bioinformatic analysis on the latter mutation suggested that it could correspond to a deleterious mutation because it is in a highly conserved domain of the sulfate transporter. |
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