"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 |
| 2013 | 1 | 0 | 1 |
| 2015 | 2 | 0 | 2 |
| 2020 | 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.
-
Bizzell E, Ross J, Rosenthal C, Dumont R, Schaaf R. Sensory Features as a Marker of Autism Spectrum Disorders. J Autism Dev Disord. 2020 Jun; 50(6):2240-2246.
-
Dhakar MB, Ilyas M, Jeong JW, Behen ME, Chugani HT. Frontal Aslant Tract Abnormality on Diffusion Tensor Imaging in an Aphasic Patient With 49, XXXXY Syndrome. Pediatr Neurol. 2016 Feb; 55:64-7.
-
Ross JL, Tartaglia N, Merry DE, Dalva M, Zinn AR. Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features. Genes Brain Behav. 2015 Feb; 14(2):137-44.
-
Bardsley MZ, Kowal K, Levy C, Gosek A, Ayari N, Tartaglia N, Lahlou N, Winder B, Grimes S, Ross JL. 47,XYY syndrome: clinical phenotype and timing of ascertainment. J Pediatr. 2013 Oct; 163(4):1085-94.
-
Haverty CE, Lin AE, Simpson E, Spence MA, Martin RA. 47,XXX associated with malformations. Am J Med Genet A. 2004 Feb 15; 125A(1):108-11; author reply 112.