Incontinentia pigmenti in a male infant with Klinefelter syndrome

Incontinentia pigmenti is a familial disorder affecting tissues derived from neuroectoderm. Statistical analysis of reported pedigrees is consistent with transmission of incontinentia pigmenti by an X-Iinked dominant gene with male hemizygote lethality. This report describes a male infant with the c...

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Veröffentlicht in:	Journal of the American Academy of Dermatology 1989-05, Vol.20 (5), p.937-940
Hauptverfasser:	Prendiville, J.S., Gorski, Jerome L., Stein, Constance K., Esterly, Nancy Burton
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Genetic Linkage Gynecology. Andrology. Obstetrics Humans Incontinentia Pigmenti - complications Incontinentia Pigmenti - genetics Infant Klinefelter Syndrome - complications Klinefelter Syndrome - diagnosis Male Male genital diseases Medical sciences Non tumoral diseases Pigmentation Disorders - genetics X Chromosome
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