Cargando…
ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants
BACKGROUND: Leukodystrophies are the main subgroup of inherited CNS white matter disorders which cause significant mortality and morbidity in early years of life. Diagnosis is mostly based on clinical context and neuroimaging findings; however, genetic tools, particularly whole-exome sequencing (WES...
Autores principales: | Dehnavi, Ali Zare, Heidari, Erfan, Rasulinezhad, Maryam, Heidari, Morteza, Ashrafi, Mahmoud Reza, Hosseini, Mohammad Mahdi, Sadeghzadeh, Fatemeh, Fallah, Mohammad-Sadegh, Rostampour, Noushin, Bahraini, Amir, Garshasbi, Masoud, Tavasoli, Ali Reza |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287746/ https://www.ncbi.nlm.nih.gov/pubmed/34281620 http://dx.doi.org/10.1186/s40246-021-00345-0 |
Ejemplares similares
-
Follow‐up of 25 patients with treatable ataxia: A comprehensive case series study
por: Ashrafi, Mahmoud Reza, et al.
Publicado: (2022) -
Expanding the genetic spectrum of giant axonal neuropathy: Two novel variants in Iranian families
por: Ashrafi, Mahmoud Reza, et al.
Publicado: (2023) -
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
por: Dehnavi, Ali Zare, et al.
Publicado: (2023) -
Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
por: Dehnavi, Ali Zare, et al.
Publicado: (2023) -
RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant
por: Kameli, Reyhaneh, et al.
Publicado: (2019)