Csécsei K, Szeifert G, Nemes Z, Tóth Z, Vachter J, Papp Z
Prog Clin Biol Res. 1982;104:505-18.
A case of prenatally diagnosed thanatophoric dysplasia is presented. Other syndromes accompanied by chondrodysplastic tetramicromelia were excluded and diagnosis was based on the narrow thorax, secondary pulmonary hypoplasia and macrocephaly detected by ultrasound and on radiological findings of disturbances of bone formation. At the mother's request labour was induced and radiological, anatomic and histological examination of the newborn confirmed the prenatal diagnosis. By electron microscopy, large conspicuous, homogeneous intracytoplasmic, usually single vacuoles were found in virtually every chondrocyte. Attention is focused on the significant hydramnion which led to the suspicion of fetal malformation. The importance of routine ultrasound screening in pregnancy is emphasised, since such malformations can be detected as early as the midtrimester pregnancy. The use of such methods ensures better maternal care.
本文报告1例产前诊断的致死性骨发育不全病例。排除了其他伴有软骨发育异常性四肢短小的综合征,诊断依据为超声检查发现的胸廓狭窄、继发性肺发育不全和巨头畸形,以及骨形成紊乱的影像学表现。应母亲要求实施引产,新生儿的影像学、解剖学和组织学检查证实了产前诊断。通过电子显微镜检查,几乎在每个软骨细胞中都发现了大的、明显的、均匀的胞质内空泡,通常为单个空泡。重点关注导致胎儿畸形怀疑的显著羊水过多。强调孕期常规超声筛查的重要性,因为此类畸形早在孕中期即可被检测到。使用此类方法可确保更好的孕产妇护理。