 Spinal Muscular Atrophies of Childhood
"Spinal Muscular Atrophies of Childhood" 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.
A group of recessively inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)
| Descriptor ID |
D014897
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| MeSH Number(s) |
C10.228.854.468.800 C10.574.500.812 C10.574.562.500.750 C10.668.467.500.750 C10.668.475.500 C16.320.400.765
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| Concept/Terms |
Juvenile Spinal Muscular Atrophy- Juvenile Spinal Muscular Atrophy
- Kugelberg-Welander Syndrome
- Kugelberg Welander Syndrome
- Kugelberg-Welander Syndromes
- Muscular Atrophy, Juvenile
- Atrophies, Juvenile Muscular
- Atrophy, Juvenile Muscular
- Juvenile Muscular Atrophies
- Juvenile Muscular Atrophy
- Muscular Atrophies, Juvenile
- Muscular Atrophy, Spinal, Type III
- Type III Spinal Muscular Atrophy
- Spinal Muscular Atrophy, Juvenile
- Spinal Muscular Atrophy, Mild Childhood and Adolescent Form
- Spinal Muscular Atrophy, Type 3
- Spinal Muscular Atrophy, Type III
- Kugelberg-Welander Disease
- Kugelberg Welander Disease
- Spinal Muscular Atrophy Type III
Muscular Atrophy, Spinal, Type II- Muscular Atrophy, Spinal, Type II
- Type II Spinal Muscular Atrophy
- Spinal Muscular Atrophy, Type II
- Spinal Muscular Atrophy Type 2
- Spinal Muscular Atrophy Type II
HMN (Hereditary Motor Neuropathy) Proximal Type I- HMN (Hereditary Motor Neuropathy) Proximal Type I
- Muscular Atrophy, Infantile
- Atrophies, Infantile Muscular
- Atrophy, Infantile Muscular
- Infantile Muscular Atrophies
- Infantile Muscular Atrophy
- Muscular Atrophy, Spinal, Infantile
- Muscular Atrophy, Spinal, Type I
- Proximal Hereditary Motor Neuropathy Type I
- SMA, Infantile Acute Form
- Spinal Muscular Atrophy Type I
- Spinal Muscular Atrophy, Infantile
- Spinal Muscular Atrophy, Type I
- Type I Spinal Muscular Atrophy
- Werdnig Hoffman Disease
- Hoffman Disease, Werdnig
- Hoffman Diseases, Werdnig
- Werdnig Hoffman Diseases
- Werdnig-Hoffmann Disease
- Werdnig Hoffmann Disease
- Infantile Spinal Muscular Atrophy
- Spinal Muscular Atrophy 1
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Below are MeSH descriptors whose meaning is more general than "Spinal Muscular Atrophies of Childhood".
Below are MeSH descriptors whose meaning is more specific than "Spinal Muscular Atrophies of Childhood".
This graph shows the total number of publications written about "Spinal Muscular Atrophies of Childhood" by people in UAMS Profiles by year, and whether "Spinal Muscular Atrophies of Childhood" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
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| 2024 | 0 | 1 | 1 | | 2020 | 3 | 0 | 3 | | 2011 | 0 | 1 | 1 |
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Below are the most recent publications written about "Spinal Muscular Atrophies of Childhood" by people in Profiles over the past ten years.
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Goedeker NL, Rogers A, Fisher M, Arya K, Brandsema JF, Farah H, Farrar MA, Felker MV, Gibbons M, Hamid OA, Harmelink M, Herbert K, Kichula E, King K, Lakhotia A, Lee BH, Kuntz NL, Parsons J, Rehborg R, Veerapaniyan A, Zaidman CM. Outcomes of early-treated infants with spinal muscular atrophy: A multicenter, retrospective cohort study. Muscle Nerve. 2024 Dec; 70(6):1247-1256.
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Harada Y, Rao VK, Arya K, Kuntz NL, DiDonato CJ, Napchan-Pomerantz G, Agarwal A, Stefans V, Katsuno M, Veerapandiyan A. Combination molecular therapies for type 1 spinal muscular atrophy. Muscle Nerve. 2020 10; 62(4):550-554.
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Feldman AG, Parsons JA, Dutmer CM, Veerapandiyan A, Hafberg E, Maloney N, Mack CL. Subacute Liver Failure Following Gene Replacement Therapy for Spinal Muscular Atrophy Type 1. J Pediatr. 2020 10; 225:252-258.e1.
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Stevens D, Claborn MK, Gildon BL, Kessler TL, Walker C. Onasemnogene Abeparvovec-xioi: Gene Therapy for Spinal Muscular Atrophy. Ann Pharmacother. 2020 10; 54(10):1001-1009.
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