Sconyers S M, Rimoin D L, Lachman R S, Adomian G E, Crandall B F
J Pediatr. 1983 Dec;103(6):898-904. doi: 10.1016/s0022-3476(83)80709-4.
Two sibs, one girl and one boy, were observed in infancy with a severe lethal skeletal dysplasia syndrome that radiologically and histologically resembled Kniest dysplasia but clearly differed in clinical course and inheritance. Kniest dysplasia is a nonlethal syndrome, whereas both of these infants died in the neonatal period. Kniest dysplasia appears to be inherited as an autosomal dominant trait; the likely transmission in this family was autosomal recessive. Roentgenograms revealed dumbbell-shaped long bones superficially similar to Kniest dysplasia, but with markedly shortened diaphyses and metaphyseal irregularities. Chondro-osseous morphology demonstrated a superficially similar foamy "Swiss cheese" appearance to the cartilage matrix, as seen in Kniest dysplasia, but there were distinctly different changes in the growth plate and resting cartilage. Ultrastructurally, the chondrocytic endoplasmic reticulum was found to have an appearance different from that observed in either normal or Kniest cartilage. These cases likely represent a distinct chondrodysplasia.
观察到两名同胞,一女一男,在婴儿期患有严重的致死性骨骼发育异常综合征,其放射学和组织学表现类似于克尼斯发育异常,但在临床病程和遗传方式上明显不同。克尼斯发育异常是一种非致死性综合征,而这两名婴儿均在新生儿期死亡。克尼斯发育异常似乎以常染色体显性性状遗传;该家族中可能的遗传方式为常染色体隐性遗传。X线片显示哑铃形长骨,表面上与克尼斯发育异常相似,但骨干明显缩短且干骺端不规则。软骨-骨形态学显示,软骨基质表面呈现出与克尼斯发育异常中所见相似的泡沫状“瑞士奶酪”外观,但生长板和静止软骨存在明显不同的变化。超微结构上,发现软骨细胞内质网的外观与正常或克尼斯软骨中观察到的不同。这些病例可能代表一种独特的软骨发育异常。