Association of achondroplasia with Down syndrome: Difficulty in prenatal diagnosis by sonographic and 3‐D helical computed tomographic analyses |
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Authors: | Akimune Kaga Jun Murotsuki Miki Kamimura Masato Kimura Akiko Saito‐Hakoda Junko Kanno Kazuhiko Hoshi Shigeo Kure Ikuma Fujiwara |
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Affiliation: | 1. Department of Pediatrics, Tohoku University Hospital, Sendai, Japan;2. Department of Maternal and Fetal Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan;3. Department of Obstetrics, Miyagi Children's Hospital, Sendai, Japan;4. Department of Obstetrics, Suzuki Memorial Hospital, Iwanuma, Miyagi, Japan |
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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. |
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Keywords: | achondroplasia Down syndrome fibroblast growth factor receptor 3 prenatal 3‐D helical computed tomographic analysis prenatal sonographic analysis |
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