Buschke-ollendorff syndrome: report of a case and interpretation of the clinical phenotype as a type 2 segmental manifestation of an autosomal dominant skin disease

Buschke-Ollendorff syndrome is a rare, autosomal dominant disease consisting of osteopoikilosis and skin manifestations. A case is reported, and the literature is reviewed with special reference to the clinical distribution patterns of skin lesions. The 2 main types of skin manifestations in this en...

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Veröffentlicht in:	Journal of the American Academy of Dermatology 2003-12, Vol.49 (6), p.1163-1166
Hauptverfasser:	Ehrig, Torsten, Cockerell, Clay J.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Dermatology Diseases of the osteoarticular system Female Genes, Dominant Humans Loss of Heterozygosity Malformations and congenital and or hereditary diseases involving bones. Joint deformations Medical sciences Middle Aged Osteopoikilosis - genetics Osteopoikilosis - pathology Phenotype Skin Diseases - genetics Skin Diseases - pathology
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