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Klinefelter's syndrome and incontinentia pigmenti Bloch-Sulzberger.
J Kunze, U H Frenzel, E Hüttig, Grosse F-R and Wiedemann H-R
Hum Genet 35(2):237-40 (1977)
PMID 844872
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.
DOI:
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DOI:
Version: za2963e q8za4 q8zb5 q8zc5 q8zd0 q8ze7 q8zfc q8zg0