Murano I, Ohashi H, Tsukahara M, Tonoki H, Okino F, Atsumi M, Kajii T
Department of Pediatrics, Yamaguchi University School of Medicine, Ube, Japan.
Clin Genet. 1991 Jan;39(1):68-74. doi: 10.1111/j.1399-0004.1991.tb02988.x.
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.