"Sex Chromosome Disorders" 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.
Clinical conditions caused by an abnormal sex chromosome constitution (SEX CHROMOSOME ABERRATIONS), in which there is extra or missing sex chromosome material (either a whole chromosome or a chromosome segment).
| Descriptor ID |
D025064
|
| MeSH Number(s) |
C16.131.260.830 C16.320.180.830
|
| Concept/Terms |
Sex Chromosome Disorders- Sex Chromosome Disorders
- Disorders, Sex Chromosome Abnormality
- Sex Chromosome Abnormality Disorders
- Disorders, Sex Chromosome
- Chromosome Disorder, Sex
- Chromosome Disorders, Sex
- Sex Chromosome Disorder
|
Below are MeSH descriptors whose meaning is more general than "Sex Chromosome Disorders".
Below are MeSH descriptors whose meaning is more specific than "Sex Chromosome Disorders".
This graph shows the total number of publications written about "Sex Chromosome Disorders" by people in this website by year, and whether "Sex Chromosome Disorders" 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 |
|---|
| 2004 | 1 | 0 | 1 |
| 2009 | 0 | 1 | 1 |
| 2011 | 1 | 0 | 1 |
| 2015 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Sex Chromosome Disorders" by people in Profiles.
-
Klinefelter syndrome and 47,XYY syndrome in children with B cell acute lymphoblastic leukaemia. Br J Haematol. 2017 12; 179(5):843-846.
-
Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review. BMC Med Genet. 2015 Mar 14; 16:12.
-
Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions. J Med Genet. 2011 Dec; 48(12):840-50.
-
A genome-wide screen for copy number alterations in Aicardi syndrome. Am J Med Genet A. 2009 Oct; 149A(10):2113-21.
-
HLHS with severe aortic insufficiency in a patient with 45,X/46,XY mosaicism. Ann Thorac Surg. 2004 Oct; 78(4):1475-6.
-
Genetic disorders and infertility. Urol Clin North Am. 2003 Feb; 30(1):143-52.