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Familial Amyloid Polyneuropathy, Type V
Known as:
Finnish Type Familial Amyloid Neuropathy
, Type V Familial Amyloid Polyneuropathy
, Biber haab dimmer dystrophy
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The presence of fine, branching linear opacities in Bowman's layer in the central area that may spread to the periphery in the clinical course. The…
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National Institutes of Health
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Related topics
Related topics
7 relations
Broader (3)
Amyloid Neuropathies, Familial
Corneal dystrophy
Hereditary corneal dystrophy
Amyloidosis
Corneal Dystrophy, Lattice Type IIIA
GSN gene
Lattice corneal dystrophy Type I
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Heavy-Chain Amyloidosis in TGFBI-Negative and Gelsolin-Negative Atypical Lattice Corneal Dystrophy
Monika A Pradhan
,
R. Henderson
,
Dipika V. Patel
,
C. McGhee
,
A. Vincent
Cornea
2011
Corpus ID: 25146918
Purpose: An atypical case of late-onset lattice corneal dystrophy is described in a 61-year-old man without a family history of…
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2006
2006
[Autosomal dominant granular corneal dystrophy caused by a TGFBI gene mutation in a Mexican family].
J. Zenteno
,
C. Santacruz-Valdes
,
A. Ramirez-Miranda
Archivos de la Sociedad Española de Oftalmología
2006
Corpus ID: 10014905
OBJECTIVE To describe the clinical data and the results of molecular analyses of the TGFBI gene in a patient with classic…
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2000
2000
Corneal amyloidosis caused by Leu 518 Pro mutation of â igh 3 gene
K. Hirano
,
Yoshihiro Hotta
,
K. Fujiki
,
A. Kanai
2000
Corpus ID: 262149695
Aim—To report a Japanese family diagnosed clinically as having lattice corneal dystrophy type I (LCDI) in which a Leu518Pro…
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1995
1995
Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval.
C. Gregory
,
K. Evans
,
S. Bhattacharya
Journal of Medical Genetics
1995
Corpus ID: 17290580
Lattice corneal dystrophy type I (LCDI) is a relatively common corneal dystrophy which can cause severe visual impairment. Recent…
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1988
1988
Corneal elastosis within lattice dystrophy lesions.
J. Pe’er
,
A. Dixon
,
D. S. Rothberg
,
J. Pe’er
,
A. Dixon
British Journal of Ophthalmology
1988
Corpus ID: 25363394
Corneal buttons of two patients with lattice corneal dystrophy were studied by light and electron microscopy. They showed…
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1985
1985
[Focus on an anatomoclinical entity: Biber-Haab-Dimmer lattice dystrophy].
L. Durand
,
R. Resal
,
C. Burillon
Journal Francais d'Ophtalmologie
1985
Corpus ID: 6106309
The present study tries to point out new ideas about lattice corneal dystrophy. From our own observations we distinguish five…
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1982
1982
Diagnosis of early lattice corneal dystrophy.
P. Dubord
,
J. Krachmer
A M A Archives of Ophthalmology
1982
Corpus ID: 34539729
Seven children from two unrelated families had lattice corneal dystrophy. Their ages ranged from 3 to 13 years at initial…
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1978
1978
Adult polycystic kidney disease and lattice corneal dystrophy: occurrence in a single family.
J. Whitt
,
B. C. Wood
,
J. Sharma
,
T. Crouch
Archives of Internal Medicine
1978
Corpus ID: 37414535
Most ophthalmologic disorders reported with renal cystic disease have been associated with either medullary cystic disease or…
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Review
1971
Review
1971
Current concepts on the ultrastructural pathogenesis of macular and lattice corneal dystrophies.
G. Klintworth
Birth defects original article series
1971
Corpus ID: 22933332
Some thoughts on the ultrastructural genesis of the lesions in macular and lattice corneal dystrophy are reviewed. These two…
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1967
1967
Primary familial corneal amyloidosis (lattice corneal dystrophy).
G. Klintworth
Annals of Internal Medicine
1967
Corpus ID: 40123741
Excerpt It is well established that amyloidosis may be a consequence of such disease processes as chronic sepsis, tuberculosis…
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