Shibuya Y, Tonoki H, Kajii N, Niikawa N
Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan.
Clin Genet. 1991 Sep;40(3):233-6. doi: 10.1111/j.1399-0004.1991.tb03083.x.
The origin of an extra marker chromosome in a patient with mental retardation and intractable epilepsy was ascertained by DNA analysis. Gene dose and restriction fragment length polymorphism (RFLP) studies of D15S9 proved that the patient was tetrasomic for the gene and that the extra chromosome was of maternal origin. On the basis of the molecular findings, further detailed GTG-banded chromosome analysis interpreted the marker chromosome as inv dup(15)(pter----q14::q14----pter). The clinical manifestations of the patient are consistent with those of the patients previously described.
通过DNA分析确定了一名患有智力迟钝和顽固性癫痫患者额外标记染色体的来源。对D15S9的基因剂量和限制性片段长度多态性(RFLP)研究证明,该患者该基因呈四体状态,且额外染色体源自母亲。基于分子研究结果,进一步详细的GTG带型染色体分析将标记染色体解释为inv dup(15)(pter----q14::q14----pter)。该患者的临床表现与先前描述的患者一致。