Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies.
Publication/Presentation Date
8-1-1978
Abstract
Familial primary cutaneous amyloidosis, a rare, autosomal dominant genodermatosis, affected 16 of 46 family members of German descent. Previous case reports involved families of Russian, Spanish, or Chinese descent. The finding of IgG, IgM, C3 in the amyloid deposits confirms recent reports of immunofluorescent dermal amyloid deposits.
Volume
114
Issue
8
First Page
1173
Last Page
1176
ISSN
0003-987X
Published In/Presented At
Vasily, D. B., Bhatia, S. G., & Uhlin, S. R. (1978). Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies. Archives of dermatology, 114(8), 1173–1176.
Disciplines
Medicine and Health Sciences
PubMedID
354533
Department(s)
Department of Medicine
Document Type
Article
COinS