Term Gallery logo

Значения термина hereditary spastic paraplegia на английском

русский
спастическая спинальная параплегия
португальский
paraparesia espástica familiar
каталонский
síndrome de strumpell-lorrain
испанский
paraplejia espástica familiar

Genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs.

Похожие термины
спастическая спинальная параплегия
Использование термина hereditary spastic paraplegia на английском
1
Autosomal dominant hereditary spastic paraplegia is genetically heterogeneous, with at least five loci identified by linkage analysis.
Pubmed
2
Understanding the cellular functions of spatacsin will allow deciphering mechanisms of motor cortex dysfunction in autosomal-recessive hereditary spastic paraplegia.
Pubmed
3
SPG13, an autosomal dominant form of pure hereditary spastic paraplegia, was recently mapped to chromosome 2q24-34 in a French family.
Pubmed
4
Recently, mutations in spastin were identified in SPG4, the most common locus for dominant hereditary spastic paraplegia that was previously mapped to chromosome 2p22.
Pubmed
5
Purpose of review: Hereditary spastic paraplegias are a genetically heterogeneous group of diseases.
Pubmed
6
Hereditary spastic paraplegia is a spastic gait disorder that arises from degeneration of corticospinal axons.
Pubmed
7
Hereditary spastic paraplegias are a group of inherited motor neuron diseases characterized by progressive paraparesis and spasticity.
Pubmed
8
Hereditary spastic paraplegias are a heterogeneous group of neurodegenerative disorders, clinically classified in pure and complex forms.
Pubmed
9
The hereditary spastic paraplegias are an expanding and heterogeneous group of disorders characterized by spasticity in the lower limbs.
Pubmed