 Sex Chromosome Aberrations
"Sex Chromosome Aberrations" 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.
Abnormal number or structure of the SEX CHROMOSOMES. Some sex chromosome aberrations are associated with SEX CHROMOSOME DISORDERS and SEX CHROMOSOME DISORDERS OF SEX DEVELOPMENT.
| Descriptor ID |
D012729
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| MeSH Number(s) |
C23.550.210.815 G05.365.590.175.815
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| Concept/Terms |
Sex Chromosome Aberrations- Sex Chromosome Aberrations
- Aberration, Sex Chromosome
- Aberrations, Sex Chromosome
- Chromosome Aberration, Sex
- Chromosome Aberrations, Sex
- Sex Chromosome Aberration
- Sex Chromosome Abnormalities
- Abnormality, Sex Chromosome
- Chromosome Abnormality, Sex
- Sex Chromosome Abnormality
- Abnormalities, Sex Chromosome
- Chromosome Abnormalities, Sex
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Below are MeSH descriptors whose meaning is more general than "Sex Chromosome Aberrations".
Below are MeSH descriptors whose meaning is more specific than "Sex Chromosome Aberrations".
This graph shows the total number of publications written about "Sex Chromosome Aberrations" by people in this website by year, and whether "Sex Chromosome Aberrations" 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 |
|---|
| 1993 | 0 | 1 | 1 | | 1994 | 0 | 1 | 1 | | 1995 | 0 | 2 | 2 | | 1997 | 0 | 1 | 1 | | 2002 | 3 | 0 | 3 | | 2006 | 1 | 0 | 1 | | 2008 | 1 | 0 | 1 | | 2009 | 1 | 0 | 1 | | 2010 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2016 | 0 | 1 | 1 | | 2020 | 1 | 2 | 3 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Sex Chromosome Aberrations" by people in Profiles.
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Guzewicz L, Howell S, Crerand CE, Umbaugh H, Nokoff NJ, Barker J, Davis SM. Clinical phenotype and management of individuals with mosaic monosomy X with Y chromosome material stratified by genital phenotype. Am J Med Genet A. 2021 05; 185(5):1437-1447.
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Davis SM, Soares K, Howell S, Cree-Green M, Buyers E, Johnson J, Tartaglia NR. Diminished Ovarian Reserve in Girls and Adolescents with Trisomy X Syndrome. Reprod Sci. 2020 11; 27(11):1985-1991.
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Tartaglia N, Howell S, Davis S, Kowal K, Tanda T, Brown M, Boada C, Alston A, Crawford L, Thompson T, van Rijn S, Wilson R, Janusz J, Ross J. Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention. Am J Med Genet C Semin Med Genet. 2020 06; 184(2):428-443.
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Thompson T, Howell S, Davis S, Wilson R, Janusz J, Boada R, Pyle L, Tartaglia N. Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies. Am J Med Genet C Semin Med Genet. 2020 06; 184(2):414-427.
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Wigby K, D'Epagnier C, Howell S, Reicks A, Wilson R, Cordeiro L, Tartaglia N. Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis. . 2016 11; 170(11):2870-2881.
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Tartaglia NR, Ayari N, Hutaff-Lee C, Boada R. Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY. J Dev Behav Pediatr. 2012 May; 33(4):309-18.
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Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L. A review of trisomy X (47,XXX). Orphanet J Rare Dis. 2010 May 11; 5:8.
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Tartaglia N, Borodyanskaya M, Borodyanskya M, Hall DA. Tremor in 48,XXYY syndrome. Mov Disord. 2009 Oct 15; 24(13):2001-7.
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Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. A new look at XXYY syndrome: medical and psychological features. . 2008 Jun 15; 146A(12):1509-22.
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Tsai AC, Fine CA, Yang M, Walton CS, Beischel L, Johnson JP. De novo isodicentric X chromosome: 46,X,idic(X)(q24), and summary of literature. . 2006 Apr 15; 140(8):923-30.
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