Mental Retardation, X-Linked
"Mental Retardation, 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.
A class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or aberrations in the structure of the X chromosome (SEX CHROMOSOME ABERRATIONS).
| Descriptor ID |
D038901
|
| MeSH Number(s) |
C10.597.606.643.455 C16.320.322.500 C16.320.400.525
|
| Concept/Terms |
Mental Retardation, X-Linked- Mental Retardation, X-Linked
- Mental Retardation, X Linked
- Retardation, X-Linked Mental
- X-Linked Mental Retardations
- X-Linked Mental Retardation Disorders
- X Linked Mental Retardation Disorders
- X-Linked Mental Retardation Syndromes
- X Linked Mental Retardation Syndromes
- X-Linked Mental Retardation
- X Linked Mental Retardation
|
Below are MeSH descriptors whose meaning is more general than "Mental Retardation, X-Linked".
Below are MeSH descriptors whose meaning is more specific than "Mental Retardation, X-Linked".
This graph shows the total number of publications written about "Mental Retardation, X-Linked" by people in this website by year, and whether "Mental Retardation, X-Linked" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 |
| 2017 | 3 | 0 | 3 |
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Below are the most recent publications written about "Mental Retardation, X-Linked" by people in Profiles.
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Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes. Sci Rep. 2017 06 16; 7(1):3702.
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ZC4H2 deletions can cause severe phenotype in female carriers. Am J Med Genet A. 2017 May; 173(5):1358-1363.
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Accumulated quiescent neural stem cells in adult hippocampus of the mouse model for the MECP2 duplication syndrome. Sci Rep. 2017 01 31; 7:41701.
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Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders. J Genet. 2011 Dec; 90(3):473-7.