Sánchez L M, Labarta J D, De Negrotti T C, Migliorini A M
J Med Genet. 1985 Aug;22(4):314-6. doi: 10.1136/jmg.22.4.314.
We report a boy with a trichorhinophalangeal syndrome (TRP syndrome), severe mental retardation, and transient megacephaly, whose karyotype showed complex, apparently balanced, translocations with breakpoints in bands 3q13, 8p22, 8q13, 11p12, and 11q21. The fact that cases presenting with phenotypes corresponding to the TRP II syndrome and deletions of the long arm of chromosome 8 have been recently reported prompted us to report this case to help in the clarification of the possible relation between 8q chromosomal mutation and the aetiology of TRP syndromes.
我们报告了一名患有毛发鼻指综合征(TRP综合征)、严重智力发育迟缓及短暂巨头症的男孩,其核型显示为复杂的、明显平衡的易位,断点位于3q13、8p22、8q13、11p12和11q21带。最近有报道称出现与TRP II综合征相对应的表型且伴有8号染色体长臂缺失的病例,这促使我们报告此病例,以助于阐明8q染色体突变与TRP综合征病因之间的可能关系。