Schrott H G, Sakaguchi S, Francke U, Luzzatti L, Fialkow P J
J Med Genet. 1974 Jun;11(2):201-5. doi: 10.1136/jmg.11.2.201.
The karyotype of a child with severe mental retardation, microcephaly, minor facial anomalies, and urinary tract outflow obstruction was found to be 46,XY,13q+mat. Trypsin-Giemsa banding studies showed an inherited translocation, t(4q−;13q+), in several asymptomatic members of the family including the propositus' mother. This indicates that the propositus had partial trisomy for the distal one-third of the long arm of chromosome 4. Review of the literature suggests that urinary tract and genital anomalies may be a consistent feature of this partial trisomy.
一名患有严重智力发育迟缓、小头畸形、轻微面部异常和泌尿道流出道梗阻的儿童的核型为46,XY,13q+mat。胰蛋白酶-吉姆萨带型研究显示,包括先证者母亲在内的该家族几名无症状成员存在遗传性易位t(4q−;13q+)。这表明先证者的4号染色体长臂远端三分之一存在部分三体性。文献回顾表明,泌尿道和生殖器异常可能是这种部分三体性的一个一致特征。