New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene

BACKGROUND: Trichorhinophalangeal syndrome (TRPS) is a rare autosomal dominant genetic disorder characterised by distinctive craniofacial and skeletal abnormalities. TRPS is generally associated with mutations in the TRPS1 gene at 8q23.3 or microdeletions of the 8q23.3-q24.11 region. However, three...

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Detalles Bibliográficos
Autores principales: Crippa, Milena, Bestetti, Ilaria, Perotti, Mario, Castronovo, Chiara, Tabano, Silvia, Picinelli, Chiara, Grassi, Guido, Larizza, Lidia, Pincelli, Angela Ida, Finelli, Palma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081657/
https://www.ncbi.nlm.nih.gov/pubmed/24886451
http://dx.doi.org/10.1186/1471-2350-15-52

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081657/
https://www.ncbi.nlm.nih.gov/pubmed/24886451
http://dx.doi.org/10.1186/1471-2350-15-52

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