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P03.11: Ultrasonographic features of trisomy 13

โœ Scribed by G. Esposito; R. Napolitano; M. Di Cresce; V. Donadono; M. Volo; R. Saviano; G. Tessitore; A. Sirico; P. Martinelli

Book ID
115563183
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
47 KB
Volume
40
Category
Article
ISSN
0960-7692

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Mosaic 13 trisomy due to de novo 13/13 t
Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission karyotype: 46,XX,-13,+t(13;13)(p11;q11)/46,XX,del(13)(p11)
โœ J. P. Fryns; P. Casaer; H. Berghe ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› Springer ๐ŸŒ English โš– 254 KB

A severely retarded child with multiple malformations was found to present a mosaic karyotype 46,XX, - 13,+t(13;13)(p11;q11)/46,XX,del(13)(p11), which probably originated as the result of a de novo 13/13 translocation in a parental gamete, followed by postzygotic fission of the translocation chromos