Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes

We report the prenatal diagnosis of cystic hygroma that was subsequently identified to have haploinsufficiency of the FOXF1 and FOXC2 genes via array comparative genomic hybridization (aCGH). Deletion o f these genes has previously neither been associated with cystic hygroma nor prenatally diagnosed...

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Detalles Bibliográficos
Autores principales: Garabedian, Matthew J., Wallerstein, Donna, Medina, Nubia, Byrne, James, Wallerstein, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447218/
https://www.ncbi.nlm.nih.gov/pubmed/23074687
http://dx.doi.org/10.1155/2012/490408

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447218/
https://www.ncbi.nlm.nih.gov/pubmed/23074687
http://dx.doi.org/10.1155/2012/490408

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