Paralyses, Familial Periodic
"Paralyses, Familial Periodic" 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 heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia. These conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle. They are frequently associated with fluctuations in serum potassium levels. Periodic paralysis may also occur as a non-familial process secondary to THYROTOXICOSIS and other conditions. (From Adams et al., Principles of Neurology, 6th ed, p1481)
| Descriptor ID |
D010245
|
| MeSH Number(s) |
C05.651.701 C10.668.491.650 C16.320.565.618.711 C18.452.648.618.711
|
| Concept/Terms |
Paralyses, Familial Periodic- Paralyses, Familial Periodic
- Familial Periodic Paralyses
- Periodic Paralyses, Familial
- Familial Periodic Paralysis
- Periodic Paralysis, Familial
- Paralysis, Familial Periodic
Normokalemic Periodic Paralysis- Normokalemic Periodic Paralysis
- Normokalemic Periodic Paralyses
- Paralyses, Normokalemic Periodic
- Paralysis, Normokalemic Periodic
- Periodic Paralyses, Normokalemic
- Periodic Paralysis, Normokalemic
|
Below are MeSH descriptors whose meaning is more general than "Paralyses, Familial Periodic".
- Diseases [C]
- Musculoskeletal Diseases [C05]
- Muscular Diseases [C05.651]
- Paralyses, Familial Periodic [C05.651.701]
- Nervous System Diseases [C10]
- Neuromuscular Diseases [C10.668]
- Muscular Diseases [C10.668.491]
- Paralyses, Familial Periodic [C10.668.491.650]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Metal Metabolism, Inborn Errors [C16.320.565.618]
- Paralyses, Familial Periodic [C16.320.565.618.711]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Metabolism, Inborn Errors [C18.452.648]
- Metal Metabolism, Inborn Errors [C18.452.648.618]
- Paralyses, Familial Periodic [C18.452.648.618.711]
Below are MeSH descriptors whose meaning is more specific than "Paralyses, Familial Periodic".
This graph shows the total number of publications written about "Paralyses, Familial Periodic" by people in this website by year, and whether "Paralyses, Familial Periodic" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
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Below are the most recent publications written about "Paralyses, Familial Periodic" by people in Profiles.
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Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome. Proc Natl Acad Sci U S A. 2002 May 28; 99(11):7774-9.
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Hypokalaemic, hypophosphatemic thyrotoxic periodic paralysis. Am J Kidney Dis. 1989 Mar; 13(3):247-9.