A De Novo Unbalanced Translocation t (5;7) (q33;p22) Carrying Partial Trisomy 5q and Partial Monosomy 7p.
- Author:
Jin Yeong HAN
;
Kyeong Hee KIM
;
Kyu Guen HWANG
;
Lisa G SHAFFER
- Publication Type:Original Article
- Keywords:
Trisomy 5q;
Monosomy 7p;
Unbalanced translocation
- MeSH:
Arm;
Chromosome Aberrations;
Chromosome Deletion*;
Chromosomes, Human, Pair 5;
Fluorescence;
Growth and Development;
Humans;
In Situ Hybridization;
Intellectual Disability;
Male;
Microcephaly;
Monosomy;
Paint;
Paintings;
Trisomy*
- From:Korean Journal of Clinical Pathology
1999;19(3):364-367
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Partial trisomy of the long arm of chromosome 5 distal to 5q33 is rare. Only 16 cases have so far been reported. We report on a three-year-old boy with microcephaly, growth and developmental delay, mild mental retardation, and facial dysmorphism caused by partial 5q trisomy and partial 7p monosomy. The patient has an apparently unbalanced translocation resulting from a rearrangement between chromosomes 5 and 7 (46,XY,der (7)t (5;7) (q33;p22)de novo). Fluorescence in situ hybridization with chromosome 5 and 7 painting probes and a cri-du-chat critical region probe confirmed this chromosome rearrangement. Most cases of partial trisomy 5q33-q35 described to date are due to the unbalanced transmission of a familial translocation. To the best of our knowledge, there are no previous reports of de novo unbalanced translocations of these two chromosome abnormalities together with similar breakpoints.
