Cargando…
Infantile Neuroaxonal Dystrophy in Two Cases: Siblings with Different Presentations
Infantile neuroaxonal dystrophy (INAD) is a rare recessive neurodegenerative disorder manifested by symptoms like hypotonia, extrapyramidal signs, spastic tetraplegia, vision problems, cerebellar ataxia, cognitive complications, and dementia before the age of three. Various reports evaluated the rel...
Autores principales: | ANSARI, Behnaz, NASIRI, Jafar, NAMAZI, Hamide, SEDGHI, Maryam, AFZALI, Mahdieh |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shahid Beheshti University of Medical Sciences
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531199/ https://www.ncbi.nlm.nih.gov/pubmed/36204426 http://dx.doi.org/10.22037/ijcn.v16i2.30864 |
Ejemplares similares
-
The natural history of infantile neuroaxonal dystrophy
por: Altuame, Fadie D., et al.
Publicado: (2020) -
Infantile Neuroaxonal Dystrophy: Diagnosis and Possible Treatments
por: Babin, Patricia L., et al.
Publicado: (2018) -
Quantitative susceptibility mapping (QSM) evaluation of infantile neuroaxonal dystrophy
por: Fujiwara, Takuya, et al.
Publicado: (2019) -
The infantile neuroaxonal dystrophy rating scale (INAD-RS)
por: Atwal, Paldeep S., et al.
Publicado: (2020) -
Purkinje cell neuroaxonal dystrophy similar to nervous mutant mice phenotype in two sibling kittens
por: Résibois, Anne, et al.
Publicado: (2004)