46,XY/48,XXY,+8 in a male with clinical and dermatoglyphic features of mosaic trisomy 8 syndrome

1 July 1981

journal article
research article
Published by Wiley in Clinical Genetics

Vol. 20 (1) , 60-63
https://doi.org/10.1111/j.1399-0004.1981.tb01808.x

Abstract

A 15 yr old male was referred for management of scoliosis secondary to congenital vertebral anomalies. Cytogenetic analysis was performed because of multiple congenital malformations. The patient was found to have a mosaic 46,XY/48,XXY,+8 chromosome complement with the characteristic clinical and dermatoglyphic features of mosaic trisomy 8 syndrome.

Keywords

This publication has 7 references indexed in Scilit:

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