Stiff-Person Syndrome
"Stiff-Person Syndrome" 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 condition characterized by persistent spasms (SPASM) involving multiple muscles, primarily in the lower limbs and trunk. The illness tends to occur in the fourth to sixth decade of life, presenting with intermittent spasms that become continuous. Minor sensory stimuli, such as noise and light touch, precipitate severe spasms. Spasms do not occur during sleep and only rarely involve cranial muscles. Respiration may become impaired in advanced cases. (Adams et al., Principles of Neurology, 6th ed, p1492; Neurology 1998 Jul;51(1):85-93)
Descriptor ID |
D016750
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MeSH Number(s) |
C10.114.812 C10.228.854.790 C10.668.900 C20.111.258.850
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Concept/Terms |
Stiff-Person Syndrome- Stiff-Person Syndrome
- Stiff Person Syndrome
- Syndrome, Stiff-Person
- Stiff-Man Syndrome
- Stiff Man Syndrome
- Syndrome, Stiff-Man
- Stiffman Syndrome
- Syndrome, Stiffman
- Stiff-Baby Syndrome
- Stiff-Baby Syndromes
- Syndrome, Stiff-Baby
- Syndromes, Stiff-Baby
- Congenital Stiff-Man Syndrome
- Congenital Stiff Man Syndrome
- Congenital Stiff-Man Syndromes
- Stiff-Man Syndrome, Congenital
- Stiff-Man Syndromes, Congenital
- Syndrome, Congenital Stiff-Man
- Syndromes, Congenital Stiff-Man
- Congenital Stiff-Person Syndrome
- Congenital Stiff-Person Syndromes
- Stiff-Person Syndrome, Congenital
- Stiff-Person Syndromes, Congenital
- Syndrome, Congenital Stiff-Person
- Syndromes, Congenital Stiff-Person
- Startle Syndrome
- Startle Syndromes
- Syndrome, Startle
- Syndromes, Startle
- Moersch-Woltmann Syndrome
- Moersch Woltmann Syndrome
- Syndrome, Moersch-Woltmann
- Stiff-Trunk Syndrome
- Stiff Trunk Syndrome
- Stiff-Trunk Syndromes
- Syndrome, Stiff-Trunk
- Syndromes, Stiff-Trunk
Familial Hyperekplexia- Familial Hyperekplexia
- Familial Hyperekplexias
- Hyperekplexia, Familial
- Hyperekplexias, Familial
Hereditary Hyperekplexia- Hereditary Hyperekplexia
- Hereditary Hyperekplexias
- Hyperekplexia, Hereditary
- Hyperekplexias, Hereditary
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Below are MeSH descriptors whose meaning is more general than "Stiff-Person Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Stiff-Person Syndrome".
This graph shows the total number of publications written about "Stiff-Person Syndrome" by people in this website by year, and whether "Stiff-Person Syndrome" 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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2004 | 0 | 1 | 1 | 2008 | 1 | 0 | 1 | 2019 | 0 | 1 | 1 | 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Stiff-Person Syndrome" by people in Profiles.
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Celli SI, Nash R, Money KM, Garza M, Borko TL, Mizenko C, McMenamin C, Von Geldern G, Georges G, Piquet AL. Successful Autologous Hematopoietic Stem Cell Transplant in Glycine Receptor Antibody-Positive Stiff Person Syndrome: A Case Report Neurol Neuroimmunol Neuroinflamm. 2024 03; 11(2):e200197.
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Piquet AL, Khan M, Warner JEA, Wicklund MP, Bennett JL, Leehey MA, Seeberger L, Schreiner TL, Paz Soldan MM, Clardy SL. Novel clinical features of glycine receptor antibody syndrome: A series of 17 cases. Neurol Neuroimmunol Neuroinflamm. 2019 09; 6(5):e592.
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Oskarsson B, Pelak V, Quan D, Hall D, Foster C, Galetta S. Stiff eyes in stiff-person syndrome. Neurology. 2008 Jul 29; 71(5):378-80.
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Breitinger HG, Lanig H, Vohwinkel C, Grewer C, Breitinger U, Clark T, Becker CM. Molecular dynamics simulation links conformation of a pore-flanking region to hyperekplexia-related dysfunction of the inhibitory glycine receptor. Chem Biol. 2004 Oct; 11(10):1339-50.
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