Page last updated: 2024-10-21

urea and Spastic Paraplegia, Hereditary

urea has been researched along with Spastic Paraplegia, Hereditary in 1 studies

pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.

Spastic Paraplegia, Hereditary: 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 progressive 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)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Marco-Marín, C1
Escamilla-Honrubia, JM1
Llácer, JL1
Seri, M1
Panza, E1
Rubio, V1

Reviews

1 review available for urea and Spastic Paraplegia, Hereditary

ArticleYear
Δ
    Journal of inherited metabolic disease, 2020, Volume: 43, Issue:4

    Topics: Aldehyde Dehydrogenase; Bone and Bones; Cataract; Growth Disorders; Humans; Mutation; Pedigree; Phen

2020