Taysi K, Burde R M, Rohrbaugh J R
Ann Genet. 1982;25(3):159-61.
This communication describes a 7-year-old male with growth and psychomotor retardation and dysmorphic features who has a small terminal deletion of the long arm of chromosome 7. The proband, in addition, had bilateral coloboma of the retina and choroidea which was not reported previously in patients with this rare chromosomal deletion syndrome. Our finding and available data in the literature on the association of the coloboma of the eyes with various chromosomal abnormalities points out the importance of karyotype studies in such patients, especially in the presence of concomitant extraocular findings.
本通讯报道了一名7岁男性,患有生长发育和精神运动发育迟缓以及畸形特征,其7号染色体长臂末端存在小片段缺失。此外,先证者患有双侧视网膜和脉络膜缺损,此前在这种罕见的染色体缺失综合征患者中未见报道。我们的发现以及文献中关于眼部缺损与各种染色体异常关联的现有数据指出了对此类患者进行核型研究的重要性,尤其是在存在眼外伴随表现的情况下。