Greenberg C R, Rimoin D L, Gruber H E, DeSa D J, Reed M, Lachman R S
Department of Paediatrics and Child Health, Children's Hospital, Winnipeg, Manitoba, Canada.
Am J Med Genet. 1988 Mar;29(3):623-32. doi: 10.1002/ajmg.1320290321.
Two sibs, the offspring of consanguineous parents, presented with severe short-limb dwarfism and distinct chondro-osseous, radiologic, and histologic appearance. The first sib presented at 30 wk with severe hydrops following fetal death; the second was detected by ultrasonography at 20 wk. Radiologic abnormalities included an unusual "moth-eaten" appearance of the markedly short long bones, bizzare ectopic ossification centers, and marked platyspondyly with unusual ossification centers. Marked extramedullary erythropoiesis was present in both fetuses, and chondro-osseous histology was characterized by marked disorganization of tissue with interspersed masses of cartilage, bone, and mesenchymal tissue. These sibs appear to have a distinct previously unreported autosomal recessive skeletal dysplasia, which can present as hydrops fetalis.
两名近亲父母的后代同胞表现出严重的短肢侏儒症以及独特的软骨-骨、放射学和组织学表现。第一个同胞在孕30周时出现严重水肿,随后胎儿死亡;第二个在孕20周时通过超声检查被发现。放射学异常包括明显短小的长骨呈现出不寻常的“虫蚀样”外观、奇异的异位骨化中心以及伴有异常骨化中心的明显扁平椎。两名胎儿均存在明显的髓外造血,软骨-骨组织学特征为组织明显紊乱,伴有散在的软骨、骨和间充质组织团块。这些同胞似乎患有一种此前未报道过的独特的常染色体隐性遗传性骨骼发育不良,可表现为胎儿水肿。