• Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature is a progressive gait disorder. The disease presents with progressive...
    36 KB (3,347 words) - 19:00, 17 April 2024
  • Spastic paraplegia 15 (SPG15) is a form of hereditary spastic paraplegia that commonly becomes apparent during childhood or adolescence (e.g. between ages...
    12 KB (1,282 words) - 20:42, 24 October 2024
  • Spastic paraplegia 31 is a rare type of hereditary spastic paraplegia which is characterized by sensation anomalies of the lower extremities. People with...
    7 KB (647 words) - 09:47, 16 December 2024
  • Thumbnail for ALS
    types of symptoms. Damage to the upper motor neuron typically causes spasticity including stiffness and increased tendon reflexes, and/or clonus, while...
    129 KB (13,979 words) - 20:44, 22 December 2024
  • neuron disease Hereditary motor and sensory neuropathies Spinal muscular atrophies Charcot–Marie–Tooth disease Hereditary spastic paraplegia Irobi, J; De...
    5 KB (226 words) - 22:49, 27 March 2024
  • Spastic paraplegia 6 is a rare type of hereditary spastic paraplegia characterized by muscle tone and bladder anomalies associated with pes cavus and specific...
    6 KB (493 words) - 06:01, 11 March 2023
  • Thumbnail for PLA2G6
    basal ganglia on magnetic resonance imaging. Hereditary spastic paraplegias are a diverse class of hereditary degenerative spinal cord disorders characterized...
    16 KB (1,791 words) - 05:28, 7 July 2024
  • depending on whether additional clinical features are present besides spastic paraplegia, such as optic atrophy, ataxia, peripheral neuropathy, extrapyramidal...
    31 KB (3,717 words) - 20:27, 5 December 2024
  • Thumbnail for KIF5A
    dominant spastic paraplegia 10. KIF5A has been shown to interact with KLC1. Mutations in KIF5A have been reported to cause hereditary spastic paraplegia type...
    9 KB (990 words) - 10:22, 29 December 2023
  • solubility parameters Heat shock protein Henoch–Schönlein purpura Hereditary spastic paraplegia Highly sensitive person, with high sensory processing sensitivity...
    1 KB (133 words) - 02:22, 14 April 2024
  • Warburg Micro syndrome (WARBM), a Complex Hereditary Spastic Paraplegia or RAB18 Deficiency, is a rare autosomal recessive genetic disorder characterized...
    5 KB (308 words) - 20:22, 29 October 2024
  • that is indicative of ALS, and absence of family history for Hereditary Spastic Paraplegia (HSP) and ALS. Imaging studies to rule out structural or demyelinating...
    12 KB (1,216 words) - 17:56, 2 August 2024
  • Thumbnail for Intellectual disability-spasticity-ectrodactyly syndrome
    which is characterized by severe intellectual disabilities, hereditary spastic paraplegia, and defects of the distal limbs, such as syndactyly, ectrodactyly...
    4 KB (262 words) - 16:01, 28 October 2024
  • Thumbnail for L1 syndrome
    disorders includes X-linked complicated corpus callosum dysgenesis, spastic paraplegia 1, MASA syndrome, and X-linked hydrocephalus with stenosis of the...
    33 KB (3,530 words) - 15:06, 23 October 2024
  • Thumbnail for Foot drop
    Charcot–Marie–Tooth disease, multiple sclerosis, cerebral palsy, hereditary spastic paraplegia, Guillain–Barré syndrome, Welander distal myopathy, Friedreich's...
    22 KB (2,684 words) - 10:57, 15 December 2024
  • Thumbnail for Restless legs syndrome
    Primary lateral sclerosis Pseudobulbar palsy Hereditary spastic paraplegia LMN only: Distal hereditary motor neuronopathies Spinal muscular atrophies...
    79 KB (8,406 words) - 14:03, 17 December 2024
  • Thumbnail for Machado–Joseph disease
    resemble Hereditary Spastic Paraplegia; however, more research is needed to conclude the relationship between Type V MJD and hereditary spastic paraplegia. There...
    22 KB (2,332 words) - 13:45, 18 May 2024
  • Thumbnail for Spastin
    RD (2008). "Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin". Nature. 451 (7176): 363–7. Bibcode:2008Natur...
    8 KB (1,032 words) - 05:21, 26 December 2023
  • Thumbnail for Paraplegin
    G, et al. (Jul 1998). "A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3". American Journal of Human Genetics...
    11 KB (1,256 words) - 03:38, 8 April 2024
  • ESCRT-III components can lead to neurological disorders such as hereditary spastic paraplegia (HSP). Cellular abscission, the process by which the membrane...
    24 KB (2,948 words) - 22:42, 26 September 2024
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    Technology portal Brown-Séquard syndrome Hereditary spastic paraplegia (HSP, or familial spastic paraplegia – FSP, Strümpell–Lorrain syndrome) Myelomere...
    43 KB (5,104 words) - 19:33, 18 December 2024
  • Continua Hemifacial spasm Hemispatial neglect Hereditary motor neuropathies Hereditary spastic paraplegia Heredopathia atactica polyneuritiformis Herpes...
    13 KB (1,143 words) - 14:30, 21 December 2024
  • Thumbnail for Dementia with Lewy bodies
    is not routinely recommended because there are only rare instances of hereditary DLB. Many neurodegenerative conditions share cognitive and motor symptoms...
    136 KB (14,528 words) - 02:13, 25 November 2024
  • Mesmerized.[citation needed] In 2003, Hood was diagnosed with HSP (hereditary spastic paraplegia). She is a wheelchair user. Rashith, Rahimah (26 March 2018)...
    4 KB (203 words) - 17:24, 29 October 2024
  • Thumbnail for Narrow face
    Beasley-Cohen type Granulocytopenia with immunoglobulin abnormality Hereditary spastic paraplegia 23 and 51 Intellectual disability, autosomal recessive 5 Intellectual...
    4 KB (224 words) - 07:14, 15 April 2024
  • The Super Parental Guardians, a Philippine film Spastic gait gene, causing hereditary spastic paraplegia Simon Property Group, US, NYSE symbol Society for...
    2 KB (222 words) - 01:29, 14 September 2024
  • Thumbnail for Micrognathism
    syndrome Hallermann-Streiff syndrome Hamartoma of hypothalamus Hereditary spastic paraplegia 23 Holoprosencephaly 13, X-linked Hutchinson-Gilford syndrome...
    15 KB (1,484 words) - 03:37, 9 December 2024
  • Thumbnail for SPG20
    autosomal recessive spastic paraplegia 20 (Troyer syndrome). Troyer syndrome (SPG20) is a complicated type of hereditary spastic paraplegias (HSPs). HSP is...
    11 KB (1,252 words) - 09:18, 4 January 2024
  • Thumbnail for MASA syndrome
    spectrum belonging in the group of hereditary spastic paraplegias a paraplegia known to increase stiffness spasticity in the lower limbs. This syndrome...
    9 KB (949 words) - 08:08, 27 December 2023
  • Thumbnail for Mitochondrion
    mitochondrial proteins. This is the case in Friedreich's ataxia, hereditary spastic paraplegia, and Wilson's disease. These diseases are inherited in a dominance...
    167 KB (18,403 words) - 15:34, 16 December 2024