Dyschromatosis symmetrica hereditaria: report of a sporadic case

A group of pigment disorders is included under the denomination of “dyschromatosis”. Dyschromatosis symmetrica hereditaria is a dominant autosomal genodermatosis mostly reported in Eastern countries. It has been rarely reported in nonoriental races and spontaneous cases are scarce. We report a spont...

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Veröffentlicht in:	International journal of dermatology 2010-08, Vol.49 (8), p.918-920
Hauptverfasser:	Consigli, Javier, Gómez Zanni, Maria S., Ragazzini, Luciana, Danielo, Cristian
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Biopsy Child Dermatology Family Health Humans Male Medical sciences Pigmentary diseases of the skin Pigmentation Disorders - congenital Pigmentation Disorders - genetics Pigmentation Disorders - pathology Skin - pathology
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