Bulbo-Spinal Atrophy, X-Linked
"Bulbo-Spinal Atrophy, X-Linked" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
| Descriptor ID |
D055534
|
| MeSH Number(s) |
C10.228.854.468.399 C10.574.500.175 C10.574.562.500.374 C10.668.467.500.186 C16.320.322.076
|
| Concept/Terms |
Bulbo-Spinal Atrophy, X-Linked- Bulbo-Spinal Atrophy, X-Linked
- Atrophies, X-Linked Bulbo-Spinal
- Atrophy, X-Linked Bulbo-Spinal
- Bulbo Spinal Atrophy, X Linked
- Bulbo-Spinal Atrophies, X-Linked
- X-Linked Bulbo-Spinal Atrophies
- Kennedy Disease
- Disease, Kennedy
- Kennedy Spinal and Bulbar Muscular Atrophy
- Kennedy Syndrome
- Syndrome, Kennedy
- X-Linked Bulbo-Spinal Atrophy
- X Linked Bulbo Spinal Atrophy
- X-linked Bulbospinal Muscular Atrophy
- X linked Bulbospinal Muscular Atrophy
- Kennedy's Disease
- Disease, Kennedy's
- Kennedys Disease
- X-Linked Spinal and Bulbar Muscular Atrophy
- X Linked Spinal and Bulbar Muscular Atrophy
- Bulbospinal Muscular Atrophy, X-linked
- Bulbospinal Muscular Atrophy, X linked
- Spinal And Bulbar Muscular Atrophy, X-Linked 1
- Spinal And Bulbar Muscular Atrophy, X Linked 1
|
Below are MeSH descriptors whose meaning is more general than "Bulbo-Spinal Atrophy, X-Linked".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Spinal Cord Diseases [C10.228.854]
- Muscular Atrophy, Spinal [C10.228.854.468]
- Bulbo-Spinal Atrophy, X-Linked [C10.228.854.468.399]
- Neurodegenerative Diseases [C10.574]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.574.500.175]
- Motor Neuron Disease [C10.574.562]
- Muscular Atrophy, Spinal [C10.574.562.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.574.562.500.374]
- Neuromuscular Diseases [C10.668]
- Motor Neuron Disease [C10.668.467]
- Muscular Atrophy, Spinal [C10.668.467.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.668.467.500.186]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Genetic Diseases, X-Linked [C16.320.322]
- Bulbo-Spinal Atrophy, X-Linked [C16.320.322.076]
Below are MeSH descriptors whose meaning is more specific than "Bulbo-Spinal Atrophy, X-Linked".
This graph shows the total number of publications written about "Bulbo-Spinal Atrophy, X-Linked" by people in this website by year, and whether "Bulbo-Spinal Atrophy, X-Linked" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2021 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Bulbo-Spinal Atrophy, X-Linked" by people in Profiles.
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Gromova A, Cha B, Robinson EM, Strickland LM, Nguyen N, ElMallah MK, Cortes CJ, La Spada AR. X-linked SBMA model mice display relevant non-neurological phenotypes and their expression of mutant androgen receptor protein in motor neurons is not required for neuromuscular disease. Acta Neuropathol Commun. 2023 06 02; 11(1):90.
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Lim WF, Forouhan M, Roberts TC, Dabney J, Ellerington R, Speciale AA, Manzano R, Lieto M, Sangha G, Banerjee S, Concei??o M, Cravo L, Biscans A, Roux L, Pourshafie N, Grunseich C, Duguez S, Khvorova A, Pennuto M, Cortes CJ, La Spada AR, Fischbeck KH, Wood MJA, Rinaldi C. Gene therapy with AR isoform 2 rescues spinal and bulbar muscular atrophy phenotype by modulating AR transcriptional activity. Sci Adv. 2021 08; 7(34).