Bartsch-Sandhoff M, Liersch R
Ann Genet. 1977 Dec;20(4):281-4.
Two sisters with statomotor developmental retardation microcephaly, hydrocephalus internus and externus without signs of pressure, heart defect (ventricular septal defect), early pulmonary resistance and characteristic facial changes were found to have the same unbalanced karyotype with partial trisomy 5q3300 leads to 5qter and partial monosomy 8p2300 leads to 8pter, derived from a balanced reciprocal paternal translocation: 46,XY,t(5;8)(q3300;p2300). The older girl was tested for the erythrocyte enzyme glutathion reductase. She had normal values.
发现两名患有静态运动发育迟缓、小头畸形、无颅内压迹象的内外部脑积水、心脏缺陷(室间隔缺损)、早期肺阻力及特征性面部改变的姐妹具有相同的不平衡核型,即5q3300至5qter的部分三体性和8p2300至8pter的部分单体性,源自父亲的平衡相互易位:46,XY,t(5;8)(q3300;p2300)。对年长女孩进行了红细胞酶谷胱甘肽还原酶检测,其值正常。