Trisomy 20p: case report and genetic review
- PMID: 3981145
Trisomy 20p: case report and genetic review
Abstract
Partial trisomy for the distal part of the short arm of chromosome 20 reported in a girl aged 11/2 years with typical craniofacial dysmorphies and psychomotor retardation. The trisomy resulted from a paternal translocation t(14;20) (q32.3;p11.1). The review of 25 cases of partial trisomy 20p showed that most cases (22 : 25) were due to parental translocations. Predominant involvement of small chromosomes in translocations with chromosome 20 was also detected.
Similar articles
-
Trisomy 20p due to a paternal reciprocal translocation.Ann Genet. 1983;26(2):94-7. Ann Genet. 1983. PMID: 6604493
-
Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.Congenit Anom (Kyoto). 2005 Dec;45(4):161-4. doi: 10.1111/j.1741-4520.2005.00087.x. Congenit Anom (Kyoto). 2005. PMID: 16359498
-
[Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].Monatsschr Kinderheilkd. 1991 Dec;139(12):841-3. Monatsschr Kinderheilkd. 1991. PMID: 1770961 German.
-
Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literature.Cytogenet Genome Res. 2012;136(4):308-13. doi: 10.1159/000337019. Epub 2012 Mar 17. Cytogenet Genome Res. 2012. PMID: 22433391 Review.
-
Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.Ann Genet. 1983;26(4):243-6. Ann Genet. 1983. PMID: 6364954 Review.
Publication types
MeSH terms
LinkOut - more resources
Research Materials