Valkova G, Ghenev E, Tzancheva M
Clin Genet. 1987 Mar;31(3):119-24. doi: 10.1111/j.1399-0004.1987.tb02781.x.
A four-month-old girl with facial dysmorphism, moderate mental retardation, immune deficiency (decreased IgG and IgA and absence of IgM), centromeric instability of chromosomes 1, 9, 16 and very rarely of chromosome 2, and disposition to formation of multibranched chromosomal figures, is described. The case is the fifth described with such chromosomal and immune abnormalities, which prove the existence of a new syndrome. The authors suggest an autosomal recessive inheritance.
本文描述了一名4个月大的女童,其患有面部畸形、中度智力发育迟缓、免疫缺陷(IgG和IgA降低,IgM缺失)、1号、9号、16号染色体着丝粒不稳定,2号染色体极少出现不稳定情况,且易形成多分支染色体形态。该病例是第五例被描述为具有此类染色体和免疫异常的病例,证实了一种新综合征的存在。作者认为这是常染色体隐性遗传。