A novel SMARCAL1 mutation associated with a mild phenotype of Schimke immuno-osseous dysplasia (SIOD)

BACKGROUND: Schimke immuno-osseous dysplasia (SIOD, OMIM #242900) is an autosomal-recessive pleiotropic disorder characterized by spondyloepiphyseal dysplasia, renal dysfunction and T-cell immunodeficiency. SIOD is caused by mutations in the gene SMARCAL1. CASE PRESENTATION: We report the clinical a...

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Detalles Bibliográficos
Autores principales: Santangelo, Luisa, Gigante, Maddalena, Netti, Giuseppe Stefano, Diella, Sterpeta, Puteo, Flora, Carbone, Vincenza, Grandaliano, Giuseppe, Giordano, Mario, Gesualdo, Loreto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973878/
https://www.ncbi.nlm.nih.gov/pubmed/24589093
http://dx.doi.org/10.1186/1471-2369-15-41

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973878/
https://www.ncbi.nlm.nih.gov/pubmed/24589093
http://dx.doi.org/10.1186/1471-2369-15-41

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