Duplication-deletion with partial trisomy lq and partial monosomy 3p resulting from a maternal reciprocal translocation rcp (1;3) (q32;p25).
- 1 February 1981
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 18 (1) , 64-68
- https://doi.org/10.1136/jmg.18.1.64
Abstract
A mother with a translocation rcp (1;3) (q32;p25) gave birth to a son with duplication of 1q32 leads to qter and deletion of 3p25 leads to pter. At 17 1/2 years of age, the proband was severely mentally retarded and presented a pattern of multiple minor dysmorphic stigmata and anomalies, including hypertrichosis, synophrys, ocular hypertelorism, ptosis, convergent squint, cleft uvula nad narrow palate, poorly modelled auricles, funnel chest, kyphoscoliosis, umbilical and inguinal hernias, and cubitus valgus. He had normal stature and did not have any apparent malformations.Keywords
This publication has 9 references indexed in Scilit:
- Partial trisomy 1q syndromeClinical Genetics, 2008
- Partial trisomy 1q due to tandem duplicationClinical Genetics, 1979
- Chromosome 3 Duplication q/Deletion p SyndromePediatrics, 1978
- [Secondary trisomy 1 q due to a reciprocal maternal translocation].1978
- A Patient With a Partial Deletion of the Short Arm of Chromosome 3American Journal of Diseases of Children, 1978
- Partial trisomy of the long arm of chromosome 1 due to a familial translocation t(1;10)(q32;q26)Human Genetics, 1978
- Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q-;6p+)Human Genetics, 1978
- Partial trisomy of the long arm of human chromosome 1 as demonstrated by in situ hybridization with 5S ribosomal RNAHuman Genetics, 1977
- “de novo” trisomy 1q32→1qter and monosomy 3p25→3pterHuman Genetics, 1977