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Ectopia Lentis
Known as:
Abnormality of lens position
, Congenital ectopic lens
, Ectopia Lentis [Disease/Finding]
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Displacement of the lens of the eye secondary to defective zonule formation that is present at the time of birth.
National Institutes of Health
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Related topics
Related topics
22 relations
Narrower (6)
Blepharoptosis myopia ectopia lentis
Ectopia Lentis with Ectopia of Pupil
Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism
Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis
Expand
Congenital contractural arachnodactyly
Cystathionine beta-Synthase Deficiency Disease
EHLERS-DANLOS SYNDROME, CLASSIC TYPE
Eye
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Broader (1)
Eye Abnormalities
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
ADAMTS proteins as modulators of microfibril formation and function.
D. Hubmacher
,
S. Apte
Matrix Biology
2015
Corpus ID: 39018664
Highly Cited
2012
Highly Cited
2012
Glued intrascleral fixation of posterior chamber intraocular lens in children.
D. Kumar
,
Amar Agarwal
,
D. Prakash
,
G. Prakash
,
S. Jacob
,
A. Agarwal
American journal of ophthalmology-glaucoma
2012
Corpus ID: 23125215
Review
2008
Review
2008
Ehlers-Danlos syndromes and Marfan syndrome.
B. Callewaert
,
F. Malfait
,
B. Loeys
,
A. De Paepe
Baillière's Best Practice & Research : Clinical…
2008
Corpus ID: 33077163
Review
2004
Review
2004
Ectopia lentis phenotypes and the FBN1 gene
L. Adès
,
K. Holman
,
M. Brett
,
M. Edwards
,
B. Bennetts
American Journal of Medical Genetics. Part A
2004
Corpus ID: 19069429
Mutations of the fibrillin‐1 (FBN1) gene on chromosome 15 have been described in patients with classical Marfan syndrome (MFS…
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Highly Cited
2003
Highly Cited
2003
Modified capsular tension ring for patients with congenital loss of zonular support
R. Cionni
,
R. Osher
,
D. M. Marques
,
F. F. Marques
,
M. Snyder
,
S. Shapiro
Journal of cataract and refractive surgery
2003
Corpus ID: 29783837
Review
2000
Review
2000
Genetic disorders of the elastic fiber system.
D. Milewicz
,
Z. Urban
,
C. Boyd
Matrix Biology
2000
Corpus ID: 42871317
Highly Cited
1994
Highly Cited
1994
A novel mutation of the fibrillin gene causing ectopia lentis.
L. Lönnqvist
,
A. Child
,
K. Kainulainen
,
R. Davidson
,
Lea Puhakka
,
L. Peltonen
Genomics
1994
Corpus ID: 30004708
Ectopia lentis (EL), a dominantly inherited connective tissue disorder, has been genetically linked to the fibrillin gene on…
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Review
1990
Review
1990
Hyperhomocyst(e)inemia. A common and easily reversible risk factor for occlusive atherosclerosis.
M. Malinow
Circulation
1990
Corpus ID: 39236366
H omocysteine (HCY) is a thiol-containing amino acid that results from the demethylation of methionine. HCY is readily oxidized…
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Highly Cited
1979
Highly Cited
1979
Vitreoretinal degeneration as a sign of generalized connective tissue diseases.
I. Maumenee
American journal of ophthalmology-glaucoma
1979
Corpus ID: 20996891
Highly Cited
1942
Highly Cited
1942
Fibroblastic Overgrowth of Persistent Tunica Vasculosa Lentis in Infants Born Prematurely: II. Report of Cases-Clinical Aspects.
Terry Tl
1942
Corpus ID: 204086596
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