Base de dados : MEDLINE
Pesquisa : Ectopia and do and Cristalino [Palavras]
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[PMID]:29422749
[Au] Autor:Al Somali AI; Al-Dossari FN; Emara KE; Al Habash A
[Ad] Endereço:Department of Ophthalmology, King Faisal University, Al Ahsa, Kingdom of Saudi Arabia.
[Ti] Título:Outcomes of Scleral-fixated Intraocular-lens in Children with Idiopathic Ectopia Lentis.
[So] Source:Middle East Afr J Ophthalmol;24(4):167-170, 2017 Oct-Dec.
[Is] ISSN:0975-1599
[Cp] País de publicação:India
[La] Idioma:eng
[Ab] Resumo:PURPOSE: The purpose of the study was to review the safety and stability of scleral-fixated intraocular lens (IOL) 2 years after implantation in children with idiopathic ectopia lentis (EL). METHODS: This retrospective case series enrolled children with EL managed between 2011 and 2015 at a tertiary eye hospital in the eastern of Saudi Arabia. Data were collected on age, gender, vision, isolated or syndromic pathology, intraoperative and postoperative complications, spherical equivalent refraction, and final best-corrected visual acuity (BCVA). RESULTS: The series included 18 eyes of 11 children with EL (6 males and 5 females). There were 7 bilateral and 4 unilateral cases. The median age was 3.5 years (25% quartile 1 year; range: 1-8 years). Preoperatively, fixation was absent in 3 eyes, 8 eyes were fixating but vision could not be recorded. In the remaining seven eyes, median distant visual acuity was 0.1 (25% quartile: 0.08). The median postoperative follow-up was 24 months (25% quartile, 7 months). Complications included two eyes with iris capture and one eye with lens subluxation requiring re-implantation. Postoperative BCVA was better than 20/60 in 15 (83%) eyes. At last follow-up, 6 eyes required myopic correction, 1 eye was emmetropic, and 11 eyes were hypermetropic. One eye with glaucoma was managed medically. CONCLUSION: Scleral fixated IOL in eyes of young children with EL had good visual outcomes and high stability. However, there is a high incidence of residual refractive error.
[Mh] Termos MeSH primário: Ectopia do Cristalino/cirurgia
Implante de Lente Intraocular/métodos
Lentes Intraoculares
Esclera/cirurgia
[Mh] Termos MeSH secundário: Criança
Pré-Escolar
Ectopia do Cristalino/fisiopatologia
Feminino
Seguimentos
Seres Humanos
Lactente
Masculino
Estudos Retrospectivos
Resultado do Tratamento
Acuidade Visual/fisiologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180223
[Lr] Data última revisão:
180223
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180210
[St] Status:MEDLINE
[do] DOI:10.4103/meajo.MEAJO_105_16


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[PMID]:28931008
[Au] Autor:Gehle P; Goergen B; Pilger D; Ruokonen P; Robinson PN; Salchow DJ
[Ad] Endereço:Department of Cardiology, Charité -University Medicine Berlin, Augustenburger Platz 1, Berlin, Germany.
[Ti] Título:Biometric and structural ocular manifestations of Marfan syndrome.
[So] Source:PLoS One;12(9):e0183370, 2017.
[Is] ISSN:1932-6203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: To study biometric and structural ocular manifestations of Marfan syndrome (MFS). METHODS: Observational, retrospective, comparative cohort study in a tertiary referral center on 285 MFS patients and 267 controls. Structural and biometric ocular characteristic were compared. RESULTS: MFS eyes were longer (axial length 24.25 ± 1.74 mm versus 23.89 ± 1.31 mm, p < 0.001) and had a flatter cornea than control eyes (mean keratometry 41.78 ± 1.80 diopters (D) versus 43.05 ± 1.51 D, p < 0.001). Corneal astigmatism was greater and the central cornea was thinner in MFS eyes (530.14 ± 41.31 µm versus 547.02 ± 39.18 µm, p < 0.001). MFS eyes were more myopic than control eyes (spherical equivalent -2.16 ± 3.75 D versus -1.17 ± 2.58 D, p < 0.001). Visual acuity was reduced (0.13 ± 0.25 logMAR versus 0.05 ± 0.18 logMAR, p < 0.001) and intraocular pressure was lower in MFS eyes (14.6 ± 3.4 mmHg versus 15.1 ± 3.2 mmHg, p = 0.01). Iris transillumination defects (ITD) were significantly more common in MFS eyes (odds ratio for MFS in the presence of ITD, 3.7). Ectopia lentis (EL) was only present in MFS eyes (33.4%). History of retinal detachment was significantly more common in MFS eyes. Glaucoma was equally common in both groups. CONCLUSIONS: ITD and EL are most characteristic findings in MFS. ITD and corneal curvature should be studied as diagnostic criteria for MFS. Visual acuity is reduced in MFS. MFS patients need regular eye exams to identify serious ocular complications.
[Mh] Termos MeSH primário: Síndrome de Marfan/diagnóstico
Síndrome de Marfan/patologia
[Mh] Termos MeSH secundário: Adolescente
Adulto
Idoso
Astigmatismo/complicações
Estudos de Casos e Controles
Criança
Pré-Escolar
Córnea/patologia
Ectopia do Cristalino/complicações
Feminino
Glaucoma/complicações
Seres Humanos
Lactente
Pressão Intraocular
Iris/fisiologia
Masculino
Síndrome de Marfan/complicações
Meia-Idade
Miopia/etiologia
Descolamento Retiniano/complicações
Estudos Retrospectivos
Acuidade Visual
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171020
[Lr] Data última revisão:
171020
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170921
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0183370


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[PMID]:28902597
[Au] Autor:Desai D; Tajik AJ
[Ad] Endereço:Aurora St. Luke's Medical Center, Milwaukee, WI publishing14@aurora.org.
[Ti] Título:Iridodonesis.
[So] Source:N Engl J Med;377(11):e14, 2017 Sep 14.
[Is] ISSN:1533-4406
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Ectopia do Cristalino/etiologia
Iris/fisiopatologia
Síndrome de Marfan/diagnóstico
[Mh] Termos MeSH secundário: Idoso
Ectopia do Cristalino/diagnóstico
Feminino
Seres Humanos
Síndrome de Marfan/complicações
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; VIDEO-AUDIO MEDIA
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170922
[Lr] Data última revisão:
170922
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170914
[St] Status:MEDLINE
[do] DOI:10.1056/NEJMicm1615424


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[PMID]:28902582
[Au] Autor:Sridhar J; Chang JS
[Ad] Endereço:Bascom Palmer Eye Institute, Miami, FL jsridhar@med.miami.edu.
[Ti] Título:Marfan's Syndrome with Ectopia Lentis.
[So] Source:N Engl J Med;377(11):1076, 2017 Sep 14.
[Is] ISSN:1533-4406
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Ectopia do Cristalino/etiologia
Síndrome de Marfan/complicações
[Mh] Termos MeSH secundário: Adulto
Ectopia do Cristalino/diagnóstico
Seres Humanos
Masculino
Transtornos da Visão/etiologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170922
[Lr] Data última revisão:
170922
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170914
[St] Status:MEDLINE
[do] DOI:10.1056/NEJMicm1406002


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[PMID]:28673264
[Au] Autor:Zhang Y; Jin G; Cao Q; Lin J; Lin J; Wang Y; Poh SE; Young CA; Zheng D
[Ad] Endereço:Department of Ophthalmology, Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
[Ti] Título:Distribution of axial length in Chinese congenital ectopia lentis patients: a retrospective study.
[So] Source:BMC Ophthalmol;17(1):113, 2017 Jul 03.
[Is] ISSN:1471-2415
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Congenital ectopia lentis (CEL) usually leads to refractive error and may influence the axial length development. But few investigations have reported patient demographics and the distribution of axial length (AL) before surgery in Chinese pediatric patients with CEL. To describe the distribution of AL before surgery in CEL patients and its relationship with patients' demographics, such as age, Marfan syndrome, sex, and laterality. METHODS: This retrospective study reviewed 306 CEL patients from January 1, 2006 to December 31, 2015. One eye was randomly selected from each patient if both eyes were EL. The influences of Marfan syndrome, sex, and laterality to AL in different age subgroups were evaluated and compared. The differences of the AL between groups were assessed using the student t test or paired t-test. P-values less than 0.05 were considered statistically significant. RESULTS: Two hundred forty-seven eyes were enrolled. 58.3% of all the patients had binoculus EL, 70% of all the patients were male and 36% of all the patients were diagnosed with Marfan syndrome. The mean AL of EL patients was 25.1 ± 2.5 mm. There was no statistical difference in the AL between patients with and without Marfan syndrome, and in the AL between male and female patients. There was statistical difference in AL between the EL-affected eye and the unaffected eye in monocular EL patients younger than 12 years old. CONCLUSIONS: This study suggests that AL can be influenced by CEL, but the influence of CEL may be reduced after the age of 12 years old, which will likely provide a useful reference when considering the most appropriate time of surgery.
[Mh] Termos MeSH primário: Comprimento Axial do Olho/patologia
Ectopia do Cristalino/diagnóstico
Refração Ocular
[Mh] Termos MeSH secundário: Adolescente
Criança
Pré-Escolar
China/epidemiologia
Ectopia do Cristalino/epidemiologia
Ectopia do Cristalino/fisiopatologia
Feminino
Seres Humanos
Incidência
Masculino
Estudos Retrospectivos
Acuidade Visual
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171004
[Lr] Data última revisão:
171004
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170705
[St] Status:MEDLINE
[do] DOI:10.1186/s12886-017-0508-1


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[PMID]:28591285
[Au] Autor:Çevik SG; Çevik MÖ; Özmen AT
[Ad] Endereço:Department of Ophthalmology, Sevket Yilmaz Education and Training Hospital, Bursa, Turkey.
[Ti] Título:Iris-claw intraocular lens implantation in children with ectopia lentis.
[So] Source:Arq Bras Oftalmol;80(2):114-117, 2017 Mar-Apr.
[Is] ISSN:1678-2925
[Cp] País de publicação:Brazil
[La] Idioma:eng
[Ab] Resumo:Purpose:: Artisan iris-claw lens implantation (AICLI) is a surgical technique for treating ectopia lentis. We aimed to compare visual outcomes and possible long-term complications of AICLI surgery in pediatric patients with ectopia lentis with or without a diagnosable hereditary disease. Methods:: Seventeen children with non-traumatic ectopia lentis were retros pectively classified into two groups: group 1 included children with a diagnosable hereditary disease (11 patients, 65%), and group 2 included children without any definable hereditary disease (six patients, 35%). Patients were evaluated for post-surgical refraction, best-corrected visual acuity, and clinical follow-up complications. Results:: The average follow-up time was 38 months, and the average age of the patients was 103 ± 53 months (30-196 months). Best-corrected visual acuity values were significantly increased in both groups after surgery (p<0.05). Target refraction values were achieved at a rate of 47% in group 1 and 22% in group 2. Post-surgery complications, such as lens dislocation (36%, 11 eyes of 10 patients) and hypotonia (10%, three eyes of three patients) were observed in both groups, and retinal detachments (10%, three eyes of three patients) were observed in three patients from group 1. Conclusions:: Compared with previous similar studies, this study utilized the largest pediatric patient group and had the longest post-surgery follow-up time. Moreover, it is advisable that pediatric patients with non-traumatic ectopia lentis be carefully screened for any underlying hereditary disease, especially diseases related to connective tissue metabolism.
[Mh] Termos MeSH primário: Ectopia do Cristalino/cirurgia
Implante de Lente Intraocular/métodos
[Mh] Termos MeSH secundário: Adolescente
Criança
Pré-Escolar
Ectopia do Cristalino/complicações
Feminino
Seguimentos
Seres Humanos
Implante de Lente Intraocular/efeitos adversos
Subluxação do Cristalino/etiologia
Masculino
Síndrome de Marfan/complicações
Síndrome de Marfan/cirurgia
Hipotonia Muscular/etiologia
Complicações Pós-Operatórias
Refração Ocular
Descolamento Retiniano/etiologia
Estudos Retrospectivos
Resultado do Tratamento
Acuidade Visual
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170927
[Lr] Data última revisão:
170927
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170608
[St] Status:MEDLINE


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[PMID]:28296765
[Au] Autor:Wang Z; Cao Q; Jin G; Young CA; Wang Y; Zheng D
[Ad] Endereço:aState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China bDepartment of Ophthalmology, University of California, San Francisco, CA, USA.
[Ti] Título:Intermittent pupillary capture of intraocular lens after transscleral fixation in congenital ectopia lentis patient triggered by dark environment: A case report.
[So] Source:Medicine (Baltimore);96(11):e6342, 2017 Mar.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Although transscleral-fixated intraocular lens (IOL) implantation has been the most frequently chosen treatment for patients with inadequate capsule support, the ghost pupillary capture phenomenon did not cause enough attention. PATIENT CONCERNS: We present an unusual case withintermittent pupillary capture of intraocular lens. DIAGNOSIS: After 5 minutes staying in the dark environment, the pentacam examination revealed a mild nasal pupillary capture of the IOL. INTERVENTIONS: A clear observation using the slit-lamp was attempted, and the light shining on the pupil sped up the sliding of the captured IOL. OUTCOMES: The captured portion of the IOL recovered rapidly accompanied with pupil retraction when the patient was exposed in the light. CONCLUSIONS: Pupillary capture of an IOL is an uncommon but potentially serious postoperative complication of transscleral fixation. Many pupillary capture cases may have been overlooked in the past. Physicians should be aware of its potential side effect, recognize its clinical manifestation, and knowledgeable of effective management.
[Mh] Termos MeSH primário: Ectopia do Cristalino/cirurgia
Implante de Lente Intraocular/efeitos adversos
Lentes Intraoculares/efeitos adversos
Complicações Pós-Operatórias/fisiopatologia
Distúrbios Pupilares/etiologia
Distúrbios Pupilares/fisiopatologia
[Mh] Termos MeSH secundário: Criança
Escuridão
Feminino
Seres Humanos
Lâmpada de Fenda
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170410
[Lr] Data última revisão:
170410
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170316
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000006342


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[PMID]:28125844
[Au] Autor:De Maria A; Wilmarth PA; David LL; Bassnett S
[Ad] Endereço:Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri, United States.
[Ti] Título:Proteomic Analysis of the Bovine and Human Ciliary Zonule.
[So] Source:Invest Ophthalmol Vis Sci;58(1):573-585, 2017 Jan 01.
[Is] ISSN:1552-5783
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Purpose: The zonule of Zinn (ciliary zonule) is a system of fibers that centers the crystalline lens on the optical axis of the eye. Mutations in zonule components underlie syndromic conditions associated with a broad range of ocular pathologies, including microspherophakia and ectopia lentis. Here, we used HPLC-mass spectrometry to determine the molecular composition of the zonule. Methods: Tryptic digests of human and bovine zonular samples were analyzed by HPLC-mass spectrometry. The distribution of selected components was confirmed by immunofluorescence confocal microscopy. In bovine samples, the composition of the equatorial zonule was compared to that of the hyaloid zonule and vitreous humor. Results: The 52 proteins common to the zonules of both species accounted for >95% of the zonular protein. Glycoproteins constituted the main structural components, with two proteins, FBN1 and LTBP2, constituting 70%-80% of the protein. Other abundant components were MFAP2, EMILIN-1, and ADAMTSL-6. Lysyl oxidase-like 1, a crosslinking enzyme implicated in collagen and elastin biogenesis, was detected at significant levels. The equatorial and hyaloid zonular samples were compositionally similar to each other, although the hyaloid sample was relatively enriched in the proteoglycan opticin and the fibrillar collagens COL2A1, COL11A1, COL5A2, and COL5A3. Conclusions: The zonular proteome was surprisingly complex. In addition to structural components, it contained signaling proteins, protease inhibitors, and crosslinking enzymes. The equatorial and hyaloid zonules were similar in composition, but the latter may form part of a composite structure, the hyaloid membrane, that stabilizes the vitreous face.
[Mh] Termos MeSH primário: Cristalino/metabolismo
Proteínas dos Microfilamentos/metabolismo
Proteômica/métodos
[Mh] Termos MeSH secundário: Adulto
Idoso
Animais
Bovinos
Cromatografia Líquida
Feminino
Seres Humanos
Cristalino/ultraestrutura
Masculino
Microscopia Confocal
Microscopia Eletrônica de Varredura
Meia-Idade
Corpo Vítreo/metabolismo
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Microfilament Proteins)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170623
[Lr] Data última revisão:
170623
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170127
[St] Status:MEDLINE
[do] DOI:10.1167/iovs.16-20866


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[PMID]:28087083
[Au] Autor:Ndoye Roth PA; Toure SA; Kane H; Sow AS; Wane AM; Ndiaye JM; Ka AM; Diagne JP; Diallo HM; Demedeiros Quenum ME; Nguer M; Ba EA; Ndiaye PA; Ndiaye MR
[Ad] Endereço:Clinique ophtalmologique, hôpital Aristide Le Dantec, 30, avenue Pasteur, 12900 Dakar, Sénégal.
[Ti] Título:[Isolated microspherophakia in a Senegalese family].
[Ti] Título:Microsphérophakie isolée dans une famille sénégalaise..
[So] Source:J Fr Ophtalmol;40(2):110-114, 2017 Feb.
[Is] ISSN:1773-0597
[Cp] País de publicação:France
[La] Idioma:fre
[Ab] Resumo:PURPOSE: To report the clinical investigation of isolated microspherophakia involving a Senegalese family in order to appreciate its functional impact. OBSERVATIONS: This is a rural family comprised of 7 members. The sibship included three girls and two boys. One of the girls, who lived in a distant zone, was unable to be examined. Of all the examined members of the family, only the father was unaffected by the illness. There was no consanguinity. The general medical examination was normal. The best-corrected visual acuity (VA) for the girls was 2/10. For one of the boys, BCVA was 8/10 for both eyes, and for the other, BCVA was 10/10 for the right eye and 8/10 for the left eye. The mother's VA was 10/10 and P2 without correction. Myopia and astigmatism were present in the 4 children of the sibship. During the examination, we noted the presence of small crystalline lenses, which were very round and presented an abnormal visibility of the lens equator and zonular fibers. The diagnosis of microspherophakia was confirmed by measurement of the lens diameters by ultrasound biomicroscopy. Complications were present in the girls, including pupillary block glaucoma and amblyopia for the elder, and retinal degeneration and amblyopia for the younger daughter. The elder daughter was managed medically with glaucoma drops. The younger daughter received optical correction and a prophylactic Argon LASER treatment. The two boys received optical correction. No treatment was recommended for the mother. CONCLUSION: Microspherophakia is a rare condition. Some serious complications can lead to amblyopia. A better multidisciplinary evaluation would allow for early detection and a better prognosis.
[Mh] Termos MeSH primário: Doenças da Córnea/patologia
Ectopia do Cristalino/patologia
Glaucoma/patologia
Iris/anormalidades
[Mh] Termos MeSH secundário: Adolescente
Adulto
Criança
Doenças da Córnea/genética
Ectopia do Cristalino/genética
Família
Feminino
Glaucoma/genética
Seres Humanos
Iris/patologia
Masculino
Senegal
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170926
[Lr] Data última revisão:
170926
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170115
[St] Status:MEDLINE


  10 / 445 MEDLINE  
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[PMID]:27709371
[Au] Autor:Rabie HM; Malekifar P; Javadi MA; Roshandel D; Esfandiari H
[Ad] Endereço:Ophthalmic Research Center, Ophthalmology Department, Labbafinejad Medical Center, Shahid Beheshti University of Medical Sciences, Pasdaran Ave. Boostan 9 St., Tehran, 1666694516, Iran.
[Ti] Título:Visual outcomes after lensectomy and iris claw artisan intraocular lens implantation in patients with Marfan syndrome.
[So] Source:Int Ophthalmol;37(4):1025-1030, 2017 Aug.
[Is] ISSN:1573-2630
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:PURPOSE: To review our experience with crystalline lens extraction and iris claw Artisan IOL implantation in patients with lens subluxation secondary to Marfan syndrome. METHODS: A retrospective analysis of 12 eyes of 9 patients with lens subluxation due to Marfan syndrome who underwent crystalline lens removal and Artisan IOL (Ophtec, Groningen, Netherlands) implantation. A questionnaire of pre- and post-operative data, including demographics, pre- and postoperative comorbidities and complications was completed. Patients were evaluated for visual outcome and occurrence of complications. Uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA), and spherical equivalents (SE) were compared before and after lens extraction and IOL insertion. RESULTS: The mean age of the participants was 30.03 ± 15.02 years, and mean post-operative follow-up time was 44.5 ± 16.4 months. Mean BCVA also showed a significant improvement from 0.5 ± 0.3 at the baseline to 0.2 ± 0.2 post-operatively (P = 0.006). SE changed significantly from -11.38 ± 1.99 preoperatively to -0.45 ± 1.65 post-operatively (P = 0.003). All eyes had the IOL implanted at desired position. Post-operative complications were retinal detachment in one case and IOL dislocation in another patient. No other complication such as ocular hypertension, angle abnormalities, clinical cystoids macular edema, and corneal decompensation was observed during the follow-up period. CONCLUSION: Artisan IOL implantation after lens extraction appears to be an attractive alternative for optical correction in cases of Marfan syndrome with ectopia lentis. It confers a significant improvement in visual acuity with reasonable risk profile.
[Mh] Termos MeSH primário: Extração de Catarata/métodos
Catarata/etiologia
Iris/cirurgia
Implante de Lente Intraocular/métodos
Lentes Intraoculares
Síndrome de Marfan/complicações
Acuidade Visual
[Mh] Termos MeSH secundário: Adolescente
Adulto
Catarata/diagnóstico
Criança
Feminino
Seguimentos
Seres Humanos
Masculino
Síndrome de Marfan/diagnóstico
Desenho de Prótese
Estudos Retrospectivos
Fatores de Tempo
Resultado do Tratamento
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171109
[Lr] Data última revisão:
171109
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161007
[St] Status:MEDLINE
[do] DOI:10.1007/s10792-016-0366-5



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