| Literature DB >> 25385298 |
Akimune Kaga1, Jun Murotsuki, Miki Kamimura, Masato Kimura, Akiko Saito-Hakoda, Junko Kanno, Kazuhiko Hoshi, Shigeo Kure, Ikuma Fujiwara.
Abstract
Achondroplasia and Down syndrome are relatively common conditions individually. But co-occurrence of both conditions in the same patient is rare and there have been no reports of fetal analysis of this condition by prenatal sonographic and three-dimensional (3-D) helical computed tomography (CT). Prenatal sonographic findings seen in persons with Down syndrome, such as a thickened nuchal fold, cardiac defects, and echogenic bowel were not found in the patient. A prenatal 3-D helical CT revealed a large head with frontal bossing, metaphyseal flaring of the long bones, and small iliac wings, which suggested achondroplasia. In a case with combination of achondroplasia and Down syndrome, it may be difficult to diagnose the co-occurrence prenatally without typical markers of Down syndrome.Entities:
Keywords: Down syndrome; achondroplasia; fibroblast growth factor receptor 3; prenatal 3-D helical computed tomographic analysis; prenatal sonographic analysis
Mesh:
Year: 2015 PMID: 25385298 DOI: 10.1111/cga.12097
Source DB: PubMed Journal: Congenit Anom (Kyoto) ISSN: 0914-3505 Impact factor: 1.409