Familial primary cutaneous amyloidosis. Clinical, genetic, and immunofluorescent studies
D. B. Vasily, S. G. Bhatia and S. R. Uhlin
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.
