VS Yellore, B Sonmez, SA Rayner, AJ Aldave - British Journal of Ophthalmology, 2008 - bjo.bmj.com Corneal dystrophies have traditionally been defined as bilateral, symmetric
disorders that, with a few notable exceptions, are associated with autosomal
dominant inheritance and complete penetrance. The characteristic clinical ... Related articles - All 3 versions
TY Tanhehco, DE Eifrig Jr, IR Schwab, CJ … - Archives of Ophthalmology, 2006 - Am Med Assoc Reis-Bücklers corneal dystrophy (RBCD) is an inherited corneal disorder that
was first described by Reis 1 in 1917 and later by Bücklers 2 in 1949. Affected
individuals have an onset early in life and have frequently recurring, ... Cited by 5 - Related articles - BL Direct - All 4 versions
AJ Aldave, DY Lin, AH Principe, VS Yellore, … - American journal of ophthalmology, 2004 - Elsevier A 58-year-old man with a history of recurrent corneal erosions was diagnosed
with bilateral anterior basement membrane dystrophy and unilateral lattice
corneal dystrophy. All 17 exons of the TGFBI gene were screened for ... Cited by 5 - Related articles - All 7 versions
AJ Aldave, AH Principe, DY Lin, VS Yellore, … - Cornea, 2005 - journals.lww.com Skip Navigation Links Home > January 2005 - Volume 24 - Issue 1 > Lattice
Dystrophy-like Localized Amyloidosis of the Cornea S... ... From the Cornea
Service, The Jules Stein Eye Institute, University of California Los ... Cited by 6 - Related articles - All 3 versions
AJ Aldave, SA Rayner, BT Kim, A Prechanond, … - Mol Vis, 2006 - molvis.org Methods: A 63-year-old man presenting with the complaint of decreased vision in
one eye was noted to have a unilateral lattice corneal dystrophy. Examination of
the patient's wife and two sons, ages 20 and 27 years old, failed to reveal ... Cited by 10 - Related articles - Cached - All 3 versions
AS Nakagawa, K Fujiki, Y Enomoto, A … - Nippon Ganka Gakkai Zasshi, 2004 - ncbi.nlm.nih.gov PURPOSE: To report a case of lattice corneal dystrophy (LCD) with Asn544Ser
(N544S) mutation of the transforming growth factor beta-induced (TGFBI) gene.
CASE: A 68-year-old male patient with late-onset, sporadic LCD without ... Cited by 10 - Related articles - BL Direct
[CITATION] The clinical utility of genetic analysis in the diagnosis and management of inherited corneal …
AJ Aldave, SA Rayner, JA King, AK Salem, A … - Cornea, 2006 - journals.lww.com Purpose: To determine whether primary, polymorphic, corneal amyloid deposition
is associated with a mutation of the TGFBI gene. Methods: Interventional case
series of 8 patients. Slit lamp exam- ination of all patients and ... Cited by 2 - Related articles - BL Direct - All 4 versions
KM Kamal, SA Rayner, MC Chen, AJ Aldave - Cornea, 2009 - journals.lww.com Results: A 65-year-old man demonstrated bilateral linear branching corneal
stromal opacities characteristic of classic LCD. No mutations were found in any
of the 17 exons of TGFBI or in the intron–exon boundary regions. Four ... Related articles - All 3 versions
