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Pigmentary dysplasias in long survivors with mosaic trisomy 18: report of two cases.

作者信息

Murano I, Ohashi H, Tsukahara M, Tonoki H, Okino F, Atsumi M, Kajii T

机构信息

Department of Pediatrics, Yamaguchi University School of Medicine, Ube, Japan.

出版信息

Clin Genet. 1991 Jan;39(1):68-74. doi: 10.1111/j.1399-0004.1991.tb02988.x.

Abstract

We describe two patients, a 19-year-old girl and a 19-year-old boy, with mosaic trisomy 18 and pigmentary dysplasias. Both patients had profound growth and mental retardation, marked kyphoscoliosis, bushy eyebrows, bulbous nose, simple ears, and joint contractures - clinical manifestations of long survivors with mosaic or non-mosaic trisomy 18. In addition, the boy showed total asymmetry. Pigmentary dysplasias of the skin with hypopigmented whorls and streaks, initially absent or overlooked at the ages 2 and 15 years, were detected on close examination. It is advisable to check closely every long survivor with mosaic or purportedly non-mosaic trisomy 18 for pigmentary dysplasias.

摘要

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