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Trisomy 20 Characterizes a Second Group of Desmoid Tumors

✍ Scribed by P. Dal Cin; R. Sciot; B. Van Damme; I. De Wever; H. Van Den Berghe

Book ID
113253380
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
62 KB
Volume
79
Category
Article
ISSN
0165-4608

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Trisomy 20 is a primary chromosome aberr
Trisomy 20 is a primary chromosome aberration in desmoid tumors
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Cytogenetic analysis revealed trisomy 20 in 4 desmoid tumors: in 2 cases as the sole aberration, in I together with +X, -Y and -I 3 and in I with +8 and a supernumerary marker chromosome. Our findings indicate that gain of chromosome 20 is an early event in the development of a large subset of desmo

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## Abstract This is a report of a trisomy 18 patient who developed Wilms tumor in conjunction with perilobar nephroblastomatosis (NB) at 9 years and 5 months of age. Review of the literature revealed that most patients with trisomy 18 who develop Wilms tumor, do so at a later than expected age for