Hengstschläger Markus, Prusa Andrea-Romana, Repa Christa, Drahonsky Regina, Deutinger Josef, Pollak Arnold, Bernaschek Gerhard
Obstetrics and Gynaecology Department, Prenatal Diagnosis and Therapy, University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria.
Dev Med Child Neurol. 2004 Jan;46(1):57-9. doi: 10.1017/s0012162204000106.
Partial trisomy of the long arm of chromosome 9 represents a very rare and heterogeneous group of chromosomal aberrations. Associated clinical features include learning disability and pyloric stenosis. We present the first patient to be reported with a duplication of the chromosome region 9q22.1-->q33. The patient (female, age 17 years) presented with growth retardation, microcephaly, facial dysmorphia, oesophageal atresia, aortic stenosis, ventricular septal defect, atrial septal defect II, hypothyroidism, and learning disability, but no pyloric stenosis. A review of all cases of partial trisomy 9q reported in the literature demonstrates that learning disability is a characteristic feature of this group of chromosomal aberrations. However, there are cases of duplications of the same chromosome 9 material, with and without pyloric stenosis. This study provides new information for future genetic counselling, especially in cases of prenatal diagnosis of partial trisomy 9q.
9号染色体长臂部分三体是一组非常罕见且异质性的染色体畸变。相关临床特征包括学习障碍和幽门狭窄。我们报告了首例9q22.1→q33染色体区域重复的患者。该患者(女性,17岁)表现为生长发育迟缓、小头畸形、面部畸形、食管闭锁、主动脉狭窄、室间隔缺损、Ⅱ型房间隔缺损、甲状腺功能减退和学习障碍,但无幽门狭窄。对文献中报道的所有9q部分三体病例的回顾表明,学习障碍是这组染色体畸变的一个特征性表现。然而,也有相同9号染色体物质重复的病例,有的伴有幽门狭窄,有的则没有。本研究为未来的遗传咨询提供了新信息,尤其是在9q部分三体的产前诊断病例中。