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Prenatal diagnosis of chondrodysplasia punctata tibia–metacarpal type using multidetector CT and three-dimensional reconstruction

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Abstract

We report a case of chondrodysplasia punctata tibia–metacarpal type (CDP-TM) that was diagnosed prenatally using multidetector CT (MDCT) with three-dimensional (3-D) CT reconstructions. Prenatal US had shown severe thoracic hypoplasia and rhizomelic shortening of the limbs, raising the suspicion of thanatophoric dysplasia. However, MDCT showed punctate calcifications in the epiphyseal cartilage of the humeri and femora, carpal bones, and paravertebral region. On 3-D CT, the tibiae were much shorter than the fibulae, the humeri were very short and bowed, and severe platyspondyly was evident. These findings led to the diagnosis of CDP-TM. The diagnosis was confirmed on postnatal radiographs. Prenatal MDCT with 3-D images may make a useful contribution to prenatal diagnosis in selected fetuses with severe skeletal dysplasia.

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Correspondence to Osamu Miyazaki.

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Miyazaki, O., Nishimura, G., Sago, H. et al. Prenatal diagnosis of chondrodysplasia punctata tibia–metacarpal type using multidetector CT and three-dimensional reconstruction. Pediatr Radiol 37, 1151–1154 (2007). https://doi.org/10.1007/s00247-007-0568-0

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  • DOI: https://doi.org/10.1007/s00247-007-0568-0

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