Velasco F, Clusellas N, Godo R M, Antich J
An Esp Pediatr. 1984 Nov 15;21(7):681-7.
A female child was found to have a partial duplication of the long arm of chromosome 14 (14q24----qter). This duplication was due to paternal balanced translocation 46,XY,t(6;14) (q27;q24). Patient had craniofacial dysmorphism with microphtalmia, flat nasal bridge, lowest malformed ears, short neck, dolicocolon and mental retardation. A comparison is made between other reported cases in the literature and this observation. Most of the anomalies described in these published reports are not shared by the present patient. This can be explained by the simultaneous presence or not of a partial deletion and the size of the duplicated segment.
一名女童被发现存在14号染色体长臂(14q24----qter)部分重复。这种重复是由于父亲的平衡易位46,XY,t(6;14) (q27;q24)。患者有颅面部畸形,伴有小眼畸形、鼻梁扁平、耳朵畸形、颈部短、乙状结肠冗长和智力发育迟缓。本文将该病例与文献中其他报道的病例进行了比较。这些已发表报告中描述的大多数异常情况该患者并未出现。这可以通过是否同时存在部分缺失以及重复片段的大小来解释。