Cargando…
Diagnostic approach in adult-onset neurometabolic diseases
Neurometabolic diseases are a group of individually rare but numerous and heterogeneous genetic diseases best known to paediatricians. The more recently reported adult forms may present with phenotypes strikingly different from paediatric ones and may mimic other more common neurological disorders i...
Autores principales: | Fernández-Eulate, Gorka, Carreau, Christophe, Benoist, Jean-François, Lamari, Foudil, Rucheton, Benoit, Shor, Natalia, Nadjar, Yann |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921565/ https://www.ncbi.nlm.nih.gov/pubmed/35140137 http://dx.doi.org/10.1136/jnnp-2021-328045 |
Ejemplares similares
-
Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era
por: Lynch, David S, et al.
Publicado: (2019) -
Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan
por: Yoshimura, Akiko, et al.
Publicado: (2019) -
Myelin oligodendrocyte glycoprotein-associated disorders are associated with HLA subtypes in a Chinese paediatric-onset cohort
por: Sun, Xiaobo, et al.
Publicado: (2020) -
Hereditary leukoencephalopathy with axonal spheroids: a spectrum of phenotypes from CNS vasculitis to parkinsonism in an adult onset leukodystrophy series
por: Lynch, David S, et al.
Publicado: (2016) -
Prospective cholestanol screening of cerebrotendinous xanthomatosis among patients with juvenile-onset unexplained bilateral cataracts
por: Fernández-Eulate, Gorka, et al.
Publicado: (2022)