Duplication of chromosome region (16)(p11.2 → p12.1) in a mother and daughter with mild mental retardation
J.J.M. Engelen, Christine de Die‐Smulders, R Dirckx, W.M.A. Verhoeven, S. Tuinier, Leopold Curfs, A.J.H. Hamers
Abstract
J.J.M. Engelen, Christine de Die‐Smulders, R Dirckx, W.M.A. Verhoeven, S. Tuinier, Leopold Curfs, A.J.H. Hamers
Abstract
We report a 40-year-old female with mild mental retardation and behavior problems and her 6-year-old daughter. Chromosome analysis showed that both patients had a proximal duplication in the short arm of chromosome 16. The aberration was characterized further with band-specific probes, resulting in a 46,XX,dir dup(16)(pter --> p11.2::p12.1 --> qter) karyotype. The clinical and cytogenetical findings are compared to other patients with partial trisomy 16p reported in the literature.
OpenAlex reports 18 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
We report a 40-year-old female with mild mental retardation and behavior problems and her 6-year-old daughter. Chromosome analysis showed that both patients had a proximal duplication in the short arm of chromosome 16. The aberration was characterized further with band-specific probes, resulting in a 46,XX,dir dup(16)(pter --> p11.2::p12.1 --> qter) karyotype. The clinical and cytogenetical findings are compared to other patients with partial trisomy 16p reported in the literature.
Key concepts: dup, Daughter, Gene duplication, Trisomy, Karyotype, Chromosome, Genetics, Chromosome analysis