 |
 |

Familial Primary Cutaneous AmyloidosisClinical, Genetic, and Immunofluorescent Studies
David B. Vasily, MD;
Shyamsunder G. Bhatia, MB, BS, DVD;
Stephen R. Uhlin, MD
Arch Dermatol. 1978;114(8):1173-1176.
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.
(Arch Dermatol 114:1173-1176, 1978)
Author Affiliations
From the Department of Dermatology, Geisinger Medical Center, Danville, Penn.
Footnotes
Accepted for publication April 5, 1978.
Reprint requests to Department of Dermatology, Geisinger Medical Center, Danville, PA 17821 (Dr Bhatia).
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
Familial Primary Localized Cutaneous Amyloidosis in Brazil
Sakuma et al.
Arch Dermatol 2009;145:695-699.
ABSTRACT
| FULL TEXT
Hereditary Amyloid Cardiomyopathy Caused by a Variant Apolipoprotein A1
Hamidi Asl et al.
Am. J. Pathol. 1999;154:221-227.
ABSTRACT
| FULL TEXT
Multiple Endocrine Neoplasia Type 2a Associated with Cutaneous Lichen Amyloidosis
Gagel et al.
ANN INTERN MED 1989;111:802-806.
ABSTRACT
Acquired Macular Pigmentation
Koch
Arch Dermatol 1986;122:463-464.
ABSTRACT
Primary Familial Cutaneous Amyloidosis: A Study of HLA Antigens in a Puerto Rican Family
De Pietro
Arch Dermatol 1981;117:639-642.
ABSTRACT
|