Whitley C B, Langer L O, Ophoven J, Gilbert E F, Gonzalez C H, Mammel M, Coleman M, Rosemberg S, Rodriques C J, Sibley R
Am J Med Genet. 1984 Oct;19(2):265-75. doi: 10.1002/ajmg.1320190209.
Fibrochondrogenesis is a rare, neonatally lethal rhizomelic chondrodysplasia distinguished from other forms of lethal dwarfism by broad long-bone metaphyses, pear-shaped vertebral bodies, and by microscopic changes of cartilage with unique interwoven fibrous septa and fibroblastic dysplasia of chondrocytes. We report the second and third well-documented cases of this apparently autosomal recessive disorder and discuss the differential diagnosis.
纤维软骨生成障碍是一种罕见的、出生时即致死的短肢型软骨发育不良,其特征为长骨骨骺增宽、椎体呈梨形,以及软骨的微观变化,表现为独特的交织纤维间隔和软骨细胞的成纤维细胞发育异常,以此与其他类型的致死性侏儒症相区分。我们报告了这一明显为常染色体隐性疾病的第二例和第三例有充分文献记录的病例,并讨论了鉴别诊断。