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Meanings of hereditary spastic paraplegia in anglès

rus
спастическая спинальная параплегия
portuguès
paraparesia espástica familiar
català
síndrome de strumpell-lorrain
espanyol
paraplejia espástica familiar

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

      Related terms
      síndrome de strumpell-lorrain
      Usage of hereditary spastic paraplegia in anglès
      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