Kunze J, Frenzel U H, Hüttig E
Hum Genet. 1977 Feb 11;35(2):237-40. doi: 10.1007/BF00393976.
We report a newborn with incontinentia pigmenti Bloch-Sulzberger and male phenotype. Chromosome analysis revealed a Klinefelter's syndrome 47,XXY. These findings are compatible with the hypothesis of dominant sexlinked genes carried on the X-chromosome in this disease.