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1 same features as those in family 2, without ectopia lentis.
2 nique for visual rehabilitation in pediatric ectopia lentis.
3 viewed, 6 (35%) had hereditary or idiopathic ectopia lentis, 5 (29%) had Marfan syndrome, 2 (12%) wer
5 the secreted metalloprotease ADAMTS17 cause ectopia lentis and short stature in humans with Weill-Ma
6 port a genetic basis for a syndromic form of ectopia lentis and the role of aspartyl hydroxylation in
7 pmental abnormalities including microcornea, ectopia lentis, and early onset of cone-rod dystrophy.
8 comparable in revised Ghent systemic score, ectopia lentis, and most phenotypic features, including
9 estations include bilateral iris hypoplasia, ectopia lentis, corectopia, ectropion uveae, and catarac
10 of dislocation in patients with a history of ectopia lentis due to Marfan syndrome, idiopathic causes
15 h suggests a possible link to other forms of ectopia lentis given that many of the genes implicated i
16 mutations cause autosomal recessive isolated ectopia lentis (IEL) and ectopia lentis et pupillae.
19 minant FBN1 mutations cause IEL or syndromic ectopia lentis (Marfan syndrome and Weill-Marchesani syn
20 nterior segment dysgenesis, Marfan syndrome, ectopia lentis, neurofibromatosis, retinal hemangioblast
21 etardation and other disabilities (including ectopia lentis, osteoporosis, and thromboembolism) in pa
22 d bilateral microcornea, childhood cataract, ectopia lentis, rhegmatogenous retinal detachment, and c
23 e postsurgical aphakia, subluxated cataract, ectopia lentis, traumatic subluxation, and decentered IO
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