锥体细胞功能不全综合征合并黄斑变性１家系３例报告马岩，彭秀芹锥体细胞功能不全综合征是一种先天性眼病，国内屡有报道，但合并黄斑变性的病例较少见，由于临床表现特殊，常不易确诊。现将本病１家系３例报告如下。例１男，２５岁，因视力差于１９９４年５月５日来诊。... Condyloma acuminatum syndrome with macular degeneration 1 family 3 cases Ma Yan, Peng Xiuqin Congenital hypoplasia syndrome is a congenital eye disease, China has repeatedly been reported, but the case of merger macular degeneration is rare, due to clinical Special performance, often difficult to diagnose. The disease is now a family of 3 cases reported as follows. Example 1 Male, 25 years old, due to poor vision in May 5, 1994 visit. ...