Cargando…
Optical genome mapping in an atypical Pelizaeus-Merzbacher prenatal challenge
Pathogenic genetic variants represent a challenge in prenatal counseling, especially when clinical presentation in familial carriers is atypical. We describe a prenatal case involving a microarray-detected duplication of PLP1 which causes X-linked Pelizaeus-Merzbacher disease, a progressive hypomyel...
Autores principales: | Rogac, Mihael, Kovanda, Anja, Lovrečić, Luca, Peterlin, Borut |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407396/ https://www.ncbi.nlm.nih.gov/pubmed/37560384 http://dx.doi.org/10.3389/fgene.2023.1173426 |
Ejemplares similares
-
Pelizaeus-Merzbacher disease in siblings
por: Mittal, Amit, et al.
Publicado: (2010) -
Suppression of proteolipid protein rescues Pelizaeus-Merzbacher
disease
por: Elitt, Matthew S., et al.
Publicado: (2020) -
A Patient With Pelizaeus-Merzbacher Disease Caused by a c.67G>A Mutation in the PLP1 Gene
por: Usman, Mohammad, et al.
Publicado: (2023) -
Clinical and mutational spectrum of Colombian patients with Pelizaeus Merzbacher Disease
por: Velasco Parra, Harvy Mauricio, et al.
Publicado: (2018) -
A genetically proven case of Pelizaeus-Merzbacher disease: Clinicoradiological clues
por: Saini, Lokesh, et al.
Publicado: (2016)