Ramer J C, Mowrey P N, Robins D B, Ligato S, Towfighi J, Ladda R L
Department of Pediatrics, Pennsylvania State University College of Medicine, Milton S. Hershey Medical Center, Hershey 17033.
Am J Med Genet. 1990 Nov;37(3):392-400. doi: 10.1002/ajmg.1320370320.
Five matings to a dir ins (6;2)(q16;q31q33) carrier have produced a high frequency (42%) of offspring with unbalanced karyotypes. Five children have the derivative chromosome 2 resulting in del (2)(q31q33) and one individual received the derivative chromosome 6 leading to dup (2)(q31q33). The findings associated with the deletion include pre- and postnatal growth retardation, developmental delay, minor facial anomalies, seizures, complex structural heart defects, and limb deficiency. Autopsy of one individual showed complex brain malformations including hydrocephalus secondary to obstruction of the foramina of Monro, extensive heterotopias and polymicrogyria, and an unusual form of total anomalous pulmonary venous return. We compare the findings in these children to those of previously reported cases and construct an overview of the range of anomalies. Apparently, no other individual with dup (2)(q31q33) has been described. We compare the physical peculiarities of our patient with those of individuals with duplications of overlapping regions of 2q.
与一名dir ins(6;2)(q16;q31q33)携带者进行的五次交配产生了高频率(42%)的核型不平衡后代。五个孩子有衍生染色体2,导致del(2)(q31q33),一个个体获得了衍生染色体6,导致dup(2)(q31q33)。与缺失相关的发现包括出生前和出生后的生长发育迟缓、发育延迟、轻微面部异常、癫痫发作、复杂的结构性心脏缺陷和肢体缺损。对一名个体的尸检显示有复杂的脑畸形,包括继发于门罗孔阻塞的脑积水、广泛的异位和多小脑回,以及一种不寻常形式的完全性肺静脉异位引流。我们将这些儿童的发现与先前报道的病例进行比较,并构建了异常范围的概述。显然,尚未描述其他dup(2)(q31q33)个体。我们将我们患者的身体特征与2q重叠区域重复个体的特征进行比较。