Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies.

Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies. Research Abstract Details 

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Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies. Abstract Text:

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.

Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies. Publishing Authors By Initials

For similar skin and connective tissue diseases: skin diseases research abstracts see: skin and connective tissue diseases: skin diseases research

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Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: Archives of dermatology

VOLUME: 114

Page Numbers: 1173-6

Journal Abbreviation: Arch Dermatol

ISSN: 0003-987X

DAY: 17

MONTH: Aug

YEAR: 1978

Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies. Information

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LANGUAGE: eng

NlmUniqueID: 372433

Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies. Keywords Mesh Terms:

KEYWORDS: Skin Diseases

MESH TERMS: genetics

Chemical & Substance for Abstract: Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies. Information

Substance Name: HLA Antigens

Registry Number: 0

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Country: UNITED STATES

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MEDLINETA: Arch Dermatol

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