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1 lar features including microspherophakia and ectopia lentis.
2 lar anterior segment dysgenesis, myopia, and ectopia lentis.
3 nique for visual rehabilitation in pediatric ectopia lentis.
4  same features as those in family 2, without ectopia lentis.
5 opathology of the globes was consistent with ectopia lentis.
6 viewed, 6 (35%) had hereditary or idiopathic ectopia lentis, 5 (29%) had Marfan syndrome, 2 (12%) wer
7 the integrity of zonules, such as uveitis or ectopia lentis; (6) eyes with extreme myopia or long axi
8  fibrillin-1, is genetically associated with ectopia lentis and alterations in height.
9  the secreted metalloprotease ADAMTS17 cause ectopia lentis and short stature in humans with Weill-Ma
10 port a genetic basis for a syndromic form of ectopia lentis and the role of aspartyl hydroxylation in
11 dissections, dislocation of the ocular lens (ectopia lentis) and skeletal abnormalities that are char
12 pmental abnormalities including microcornea, ectopia lentis, and early onset of cone-rod dystrophy.
13  comparable in revised Ghent systemic score, ectopia lentis, and most phenotypic features, including
14 estations include bilateral iris hypoplasia, ectopia lentis, corectopia, ectropion uveae, and catarac
15 of dislocation in patients with a history of ectopia lentis due to Marfan syndrome, idiopathic causes
16 d in fibrillin microfibril biogenesis, cause ectopia lentis (EL) and EL et pupillae.
17        The corneas of patients with MFS with ectopia lentis (EL) were significantly flatter and with
18 rome (MFS) presented with subluxated lenses (ectopia lentis, EL).
19 n patients were examined, including one with ectopia lentis et pupillae.
20  recessive isolated ectopia lentis (IEL) and ectopia lentis et pupillae.
21 ely studied in horses, few reports of equine ectopia lentis exist and no genetic investigations have
22 h suggests a possible link to other forms of ectopia lentis given that many of the genes implicated i
23 mutations cause autosomal recessive isolated ectopia lentis (IEL) and ectopia lentis et pupillae.
24 ons were among the most consistent features (ectopia lentis in 86%, myopia in 80%).
25 syndrome and primary open angle glaucoma and ectopia lentis in dogs.
26                                              Ectopia lentis in humans and other species is reported t
27                    Given the role of FBN1 in ectopia lentis in humans and other species, FBN1 should
28 th FBN1:p.(Ala882Val) as the likely cause of ectopia lentis in this foal, the first genetic explanati
29 ith a dominant mode of inheritance, of which ectopia lentis is a common feature.
30                                              Ectopia lentis is the dislocation of the natural crystal
31 minant FBN1 mutations cause IEL or syndromic ectopia lentis (Marfan syndrome and Weill-Marchesani syn
32 nterior segment dysgenesis, Marfan syndrome, ectopia lentis, neurofibromatosis, retinal hemangioblast
33 etardation and other disabilities (including ectopia lentis, osteoporosis, and thromboembolism) in pa
34 d bilateral microcornea, childhood cataract, ectopia lentis, rhegmatogenous retinal detachment, and c
35 e postsurgical aphakia, subluxated cataract, ectopia lentis, traumatic subluxation, and decentered IO
36 wise healthy four-year-old boy with isolated ectopia lentis whose partial lens dislocation was captur
37 t presents a unique presentation of isolated ectopia lentis with anterior lens dislocation and pupill