Source:http://linkedlifedata.com/resource/pubmed/id/16158437
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2005-9-27
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pubmed:abstractText |
Ullrich-Turner syndrome (UTS) is most commonly due to a 45,X chromosome defect, but is also seen in patients with a variety of X-chromosome abnormalities or 45,X/46,XY mosaicism. The phenotype of UTS patients is highly variable, and depends largely on the karyotype. Patients are at an increased risk of gonadoblastoma when a Y-derived chromosome or chromosome fragment is present. Since constitutional mosaicism is present in approximately 50% of UTS patients, the identification of minor cell populations is clinically important and a challenge to laboratories. We identified 50 females with a 45,X karyotype as the sole abnormality or as part of a more complex karyotype. Twenty two (44%) had a 45,X karyotype; mosaicism for a second normal or structurally abnormal X was observed in 24 (48%) samples, and mosaicism for Y chromosomal material in 4 (8%) cases. To further investigate the possibility of mosaicism in the 22 patients with an apparently non-mosaic 45,X karyotype, we performed FISH using centromere probes for the X and Y chromosomes. A minor XX cell line was identified in 3 patients, and the 45,X result was confirmed in 19 samples. No samples with XY mosaicism were identified. We describe our validation process for a FISH assay to be used in clinical practice to identify XX or XY mosaicism. FISH as an adjunct to karyotype analysis provides a sensitive and cost-effective technique to identify sex chromosome mosaicism in UTS patients.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1552-4825
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
138A
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
259-61
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pubmed:dateRevised |
2008-5-21
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pubmed:meshHeading |
pubmed-meshheading:16158437-Chromosomes, Human, X,
pubmed-meshheading:16158437-Chromosomes, Human, Y,
pubmed-meshheading:16158437-Female,
pubmed-meshheading:16158437-Humans,
pubmed-meshheading:16158437-In Situ Hybridization, Fluorescence,
pubmed-meshheading:16158437-Male,
pubmed-meshheading:16158437-Monosomy,
pubmed-meshheading:16158437-Mosaicism,
pubmed-meshheading:16158437-Turner Syndrome
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pubmed:year |
2005
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pubmed:articleTitle |
Detection of low level sex chromosome mosaicism in Ullrich-Turner syndrome patients.
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pubmed:affiliation |
Cytogenetics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55905, USA.
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pubmed:publicationType |
Journal Article
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