GORDON K. KLINTWORTH, M.D., PH.D.
This content is PDF only. Please click on the PDF icon to access.
It is well established that amyloidosis may be a consequence of such disease processes as chronic sepsis, tuberculosis, myelomatosis, rheumatoid arthritis, and regional enteritis. In contrast to these secondary and more frequent instances of amyloidosis, amyloid deposition may occur in the absence of a recognizable cause. The latter cases tend to fall into a variety of distinctive syndromes according to the location of the deposits of amyloid. In recent years it has become apparent that many of these primary forms of amyloidosis are characterized by a genetic predisposition (1, 2).
Despite the fact that inherited forms of amyloidosis are of
KLINTWORTH GK. Primary Familial Corneal Amyloidosis (Lattice Corneal Dystrophy). Ann Intern Med. 1967;66:1288–1289. doi: https://doi.org/10.7326/0003-4819-66-6-1288
Download citation file:
Published: Ann Intern Med. 1967;66(6):1288-1289.
Copyright © 2019 American College of Physicians. All Rights Reserved.
Print ISSN: 0003-4819 | Online ISSN: 1539-3704
Conditions of Use