Classical fragile-X phenotype in a female infant disclosed by comprehensive genomic studies

BACKGROUND: We describe a female infant with Fragile-X syndrome, with a fully expanded FMR1 allele and preferential inactivation of the homologous X-chromosome carrying a de novo deletion. This unusual and rare case demonstrates the importance of a detailed genomic approach, the absence of which cou...

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Detalles Bibliográficos
Autores principales: Jorge, Paula, Garcia, Elsa, Gonçalves, Ana, Marques, Isabel, Maia, Nuno, Rodrigues, Bárbara, Santos, Helena, Fonseca, Jacinta, Soares, Gabriela, Correia, Cecília, Reis-Lima, Margarida, Cirigliano, Vincenzo, Santos, Rosário
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946481/
https://www.ncbi.nlm.nih.gov/pubmed/29747568
http://dx.doi.org/10.1186/s12881-018-0589-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946481/
https://www.ncbi.nlm.nih.gov/pubmed/29747568
http://dx.doi.org/10.1186/s12881-018-0589-6

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