Cargando…
DEPDC5 variant in focal cortical dysplasia: a case report and review of the literature
Germline and 2-hit brain somatic variants in DEPDC5 gene, a negative regulator of the mammalian target of rapamycin (mTOR) pathway, are increasingly recognized in patients with focal cortical dysplasia (FCD). Next-generation targeted sequencing identified a heterozygous germline variant in DEPDC5 ge...
Autores principales: | Jesus-Ribeiro, Joana, Pereira, Cristina, Robalo, Conceição, Pereira, Daniela J, Duro, Diana, Ramos, Fabiana, Freire, António, Melo, Joana B |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143668/ https://www.ncbi.nlm.nih.gov/pubmed/34055363 http://dx.doi.org/10.1093/omcr/omab027 |
Ejemplares similares
-
Genomic and Epigenetic Advances in Focal Cortical Dysplasia Types I and II: A Scoping Review
por: Jesus-Ribeiro, Joana, et al.
Publicado: (2021) -
Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5
por: Scerri, Thomas, et al.
Publicado: (2015) -
Second‐hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA
por: Lee, Wei Shern, et al.
Publicado: (2019) -
Focal cortical dysplasia – review
por: Kabat, Joanna, et al.
Publicado: (2012) -
MRI of focal cortical dysplasia
por: Urbach, Horst, et al.
Publicado: (2021)