Classic lattice corneal dystrophy associated with monoclonal gammopathy after exclusion of a TGFBI mutation

Cornea

Volumn 28, Issue 1, 2009, Pages 97-98

  Kamal, Khairidzan M ^a   Rayner, Sylvia A ^a   Chen, Michael C ^a   Aldave, Anthony J ^a  

^a JULES STEIN EYE INSTITUTE   (United States)

Author keywords

Lattice corneal dystrophy; Monoclonal gammopathy; TGFBI

Indexed keywords

IMMUNOGLOBULIN G; PLASMA PROTEIN; BETAIG H3 PROTEIN; BETAIG-H3 PROTEIN; SCLEROPROTEIN; TRANSFORMING GROWTH FACTOR BETA;

AGED; AMYLOIDOSIS; ARTICLE; CASE REPORT; CATARACT EXTRACTION; CLINICAL FEATURE; CORNEA DYSTROPHY; CORNEA LATTICE DYSTROPHY; CORNEA OPACITY; CORNEA STROMA; DISEASE ASSOCIATION; EXON; EYE EXAMINATION; FAMILY HISTORY; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENETIC IDENTIFICATION; GENETIC SCREENING; GLARE; HUMAN; IMMUNOGLOBULIN BLOOD LEVEL; INTRON; MALE; MONOCLONAL IMMUNOGLOBULINEMIA; MYELOPROLIFERATIVE DISORDER; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ELECTROPHORESIS; SEROLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; SLIT LAMP; SPIKE; TGFB1 GENE; VISUAL ACUITY; CONGENITAL CORNEA DYSTROPHY; ELECTROPHORESIS; GENETICS; MUTATION; PARAPROTEINEMIA; PATHOLOGY;

AGED; BLOOD PROTEINS; CORNEAL DYSTROPHIES, HEREDITARY; CORNEAL OPACITY; CORNEAL STROMA; ELECTROPHORESIS; EXONS; EXTRACELLULAR MATRIX PROTEINS; GENETIC SCREENING; HUMANS; MALE; MUTATION; PARAPROTEINEMIAS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; TRANSFORMING GROWTH FACTOR BETA;

EID: 62149141789     PISSN: 02773740     EISSN: None     Source Type: Journal    
DOI: 10.1097/ICO.0b013e31818200f4     Document Type: Article

References (7)

1. Aldave AJ, Sonmez B. Elucidating the molecular genetic basis of the corneal dystrophies: are we there yet? Arch Ophthalmol. 2007;125: 177-186.
2. Aldave AJ, Lin DY, Principe AH, et al. Anterior basement membrane corneal dystrophy and pseudo-unilateral lattice corneal dystrophy in a patient with recurrent corneal erosions. Am J Ophthalmol. 2004;137: 1124-1127.
3. Aldave AJ, Principe AH, Lin DY, et al. Lattice dystrophy-like localized amyloidosis of the cornea secondary to trichiasis. Cornea. 2005;24: 112-115.
4. Aldave AJ, Rayner SA, King JA, et al. No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition. Cornea. 2006;25:413-415.
5. Garibaldi DC, Gottsch J, de la Cruz Z, et al. Immunotactoid keratopathy: a clinicopathologic case report and a review of reports of corneal involvement in systemic paraproteinemias. Surv Ophthalmol. 2005;50: 61-80.
6. Spiegel P, Grossniklaus HE, Reinhart WJ, et al. Unusual presentation of paraproteinemic corneal infiltrates. Cornea. 1990;9:81-85.
7. Tsunoda I, Awano H, Kayama H, et al. Idiopathic AA amyloidosis manifested by autonomic neuropathy, vestibulocochleopathy, and lattice corneal dystrophy. J Neurol Neurosurg Psychiatry. 1994;57:635-637.