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  Vol. 114 No. 8, August 1978 TABLE OF CONTENTS
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Familial Primary Cutaneous Amyloidosis

Clinical, 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).



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