SPASTIC PARAPLEGIA, HEREDITARY, X LINKED RECESSIVE
\spˈastɪk pˌaɹəplˈiːd͡ʒə], \spˈastɪk pˌaɹəplˈiːdʒə], \s_p_ˈa_s_t_ɪ_k p_ˌa_ɹ_ə_p_l_ˈiː_dʒ_ə]\
Definitions of SPASTIC PARAPLEGIA, HEREDITARY, X LINKED RECESSIVE
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A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progessive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64 (1):61-6; Curr Opin Neurol 1997 Aug;10 (4):313-8)
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basidiomycota
- comprises fungi bearing the spores on basidium: Gasteromycetes (puffballs); Tiliomycetes (comprising orders Ustilaginales (smuts) and Uredinales (rusts)); Hymenomycetes (mushrooms; toadstools; agarics; bracket fungi); in some classification systems considered a division of kingdom comprises fungi bearing spores on a basidium; includes Gasteromycetes (puffballs) Tiliomycetes comprising the orders Ustilaginales (smuts) and Uredinales (rusts) Hymenomycetes (mushrooms, toadstools, agarics bracket fungi).
Nearby Words
- spastic paraplegia
- spastic paraplegia hypertrophic motor sensory neuropathy
- spastic paraplegia, autosomal recessive, hereditary
- spastic paraplegia, hereditary, autosomal dominant
- spastic paraplegia, hereditary, autosomal recessive
- Spastic Paraplegia, Hereditary, X linked Recessive
- spastic paraplegia, x linked recessive, hereditary
- spastic paraplegias
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- spastic pseudobulbar dysphonias
- spastic quadriplegia