Recent advance in sialidosis / 中华神经医学杂志
Chinese Journal of Neuromedicine
; (12): 858-861, 2022.
Article
in Zh
| WPRIM
| ID: wpr-1035691
Responsible library:
WPRO
ABSTRACT
Sialidosis is a rare autosomal recessive genetic disorder, and has a series of clinical symptoms and signs caused by neuraminidase 1 ( NEU1) gene mutations. This article reviews the etiology, clinical features, diagnoses, treatments and prognoses of sialidosis in order to improve the understanding and diagnosis of this disease and reduce the misdiagnosis of this disease.
Full text:
1
Database:
WPRIM
Language:
Zh
Journal:
Chinese Journal of Neuromedicine
Year:
2022
Document type:
Article