Rivera H, Turleau C, de Grouchy J, Junien C, Despoisse S, Zucker J M
Hum Genet. 1981;59(3):211-4. doi: 10.1007/BF00283666.
Two cases of del(13)-retinoblastoma are reported. Case 1, a 13-month-old male, was monosomic due to the malsegregation of the maternal ins(20;13)(p12;q1307q14.3). The patients's sister was trisomic for 13q1307q14.3 with no evident phenotypic effect. Case 2 was a 20-month-old female with a denovo del(13)(q1303q14.3). In both instances esterase D activity showed a remarkable gene-dosage effect in monosomy, disomy, and trisomy, thus confirming the assignment of the gene locus to 13q14, and more precisely to the proximal half of this band. In all instances, the ESTD phenotypes were 1-1. It is suggested that esterase D activity should become an important diagnostic criteria for the various etiological forms of retinoblastoma.
报告了两例13号染色体缺失型视网膜母细胞瘤病例。病例1为一名13个月大的男性,由于母亲的插入染色体(20;13)(p12;q1307q14.3)发生错误分离而导致单体型。该患者的妹妹为13q1307q14.3三体,无明显表型效应。病例2是一名20个月大的女性,患有新发的13号染色体缺失(q1303q14.3)。在这两个病例中,酯酶D活性在单体型、二体型和三体型中均表现出显著的基因剂量效应,从而证实了该基因座定位于13q14,更确切地说是该带的近端一半。在所有病例中,ESTD表型均为1-1。提示酯酶D活性应成为视网膜母细胞瘤各种病因形式的重要诊断标准。