Incontinentia pigmenti in a boy with Klinefelter's syndrome
- PMID: 3612722
- PMCID: PMC1050156
- DOI: 10.1136/jmg.24.7.439
Incontinentia pigmenti in a boy with Klinefelter's syndrome
Abstract
A boy with the cutaneous lesions of incontinentia pigmenti is described. Chromosomal analysis revealed the 47,XXY karyotype of Klinefelter's syndrome. Since incontinentia pigmenti trait is usually lethal in males, the possibility of the second X chromosome protecting against fetal death is discussed.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical