Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome

BACKGROUND: KBG syndrome, a rare autosomal disorder characterised by distinctive craniofacial and skeletal features and developmental delay, is caused by haploinsufficiency of the ANKRD11 gene. RESULTS: Here we describe two siblings with multiple symptoms characteristic of KBG and their mother with...

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Detalles Bibliográficos
Autores principales: Crippa, Milena, Rusconi, Daniela, Castronovo, Chiara, Bestetti, Ilaria, Russo, Silvia, Cereda, Anna, Selicorni, Angelo, Larizza, Lidia, Finelli, Palma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383199/
https://www.ncbi.nlm.nih.gov/pubmed/25838844
http://dx.doi.org/10.1186/s13039-015-0126-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383199/
https://www.ncbi.nlm.nih.gov/pubmed/25838844
http://dx.doi.org/10.1186/s13039-015-0126-7

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