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). A second example

J P Fryns; A Kleczkowska; J Jaeken; K Van Herck; M H Van den Berghe

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). A second example

Ann Genet. 1989;32(3):177-9.

Authors

J P Fryns¹, A Kleczkowska, J Jaeken, K Van Herck, M H Van den Berghe

Affiliation

¹ Centre for Human Genetics, U.Z. Gasthuisberg, Leuven, Belgium.

PMID: 2486064

Abstract

In this paper we report a second example of 13 trisomy mosaicism due to de novo 13/13 translocation followed by postzygotic fission of the translocation chromosome in a polymalformed female newborn.

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / genetics*
Abnormalities, Multiple / pathology
Chromosome Aberrations / genetics*
Chromosome Aberrations / pathology
Chromosome Disorders
Chromosomes, Human, Pair 13 / ultrastructure*
Female
Heart Defects, Congenital / genetics
Humans
Infant, Newborn
Mitosis
Monosomy
Mosaicism*
Translocation, Genetic
Trisomy*
Viscera / abnormalities