Eteson D J, Adomian G E, Ornoy A, Koide T, Sugiura Y, Calabro A, Lungarotti S, Mastroiacovo P, Lachman R S, Rimoin D L
Am J Med Genet. 1984 Oct;19(2):277-90. doi: 10.1002/ajmg.1320190210.
Fibrochondrogenesis is a distinct, neonatally lethal, short-limb skeletal dysplasia which was first described in a single patient in 1978. We report the radiographic and morphologic studies of 2 additional unrelated stillborn infants with fibrochondrogenesis. This syndrome has distinct radiographic and chondro-osseous morphologic defects different from those seen in the other known skeletal dysplasias. The long bones are short and dumbbell-shaped with metaphyseal flare. The spine is platyspondylic with superior-inferior clefting defects, and the ribs are short and distally cupped. The growth-plate cartilage is grossly disorganized and has a densely fibrous collagenous matrix when examined by light and electron microscopy. Light, transmission, and scanning electron microscopy shows diaphyseal and metaphyseal trabecular bone to be normal.
纤维软骨发育异常是一种独特的、新生儿期致死性的短肢型骨骼发育不良,于1978年在一名患者中首次被描述。我们报告了另外2例患纤维软骨发育异常的不相关死产婴儿的影像学和形态学研究。该综合征具有与其他已知骨骼发育不良不同的独特影像学和软骨-骨形态学缺陷。长骨短且呈哑铃形,伴有干骺端增宽。脊柱椎体扁平,有上下裂缺,肋骨短且远端呈杯状。生长板软骨严重紊乱,在光镜和电镜检查下有致密的纤维胶原基质。光镜、透射电镜和扫描电镜显示骨干和干骺端小梁骨正常。