Evidence map›Paper›PMID 41088053›Full record

ArticleBMC ophthalmology2025

Ophthalmological findings in Brazilian Cornelia de Lange syndrome patients with NIPBL variants.

Thainá Vilella, Beatriz Carvalho Nunes, Giulia Steuernagel Del Valle, Isabel Furquim Pinheiro, Hiromi Aoi, Takeshi Mizuguchi, Rie Seyama, Yuri Uchiyama, Naomichi Matsumoto, Chong Ae Kim and 3 more

Abstract read
In one paragraph

Article in BMC ophthalmology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Thainá Vilella *Genetics Division, Genetics, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, São Paulo, Brazil.
Beatriz Carvalho Nunes *Genetics Division, Genetics, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, São Paulo, Brazil.
Giulia Steuernagel Del Valle *Department of Ophthalmology and Visual Sciences, Universidade Federal de São Paulo, São Paulo, Brazil.
Isabel Furquim PinheiroGenetics Unit, Instituto da Criança,, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Hiromi AoiDepartment of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Takeshi MizuguchiDepartment of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Rie SeyamaDepartment of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Yuri UchiyamaDepartment of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Naomichi MatsumotoDepartment of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Chong Ae KimGenetics Unit, Instituto da Criança,, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Juliana Maria Ferraz SallumDepartment of Ophthalmology and Visual Sciences, Universidade Federal de São Paulo, São Paulo, Brazil.
Maria Isabel Melaragno *Genetics Division, Genetics, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, São Paulo, Brazil.
Priscila Cardoso Cristovam *Department of Ophthalmology and Visual Sciences, Universidade Federal de São Paulo, São Paulo, Brazil. pccristovam@unifesp.br.

Funding

AMED JP24ek0109674, JP24ek0109760, JP24ek0109617, JP24ek0109648 and JP24ek0109677Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/21644-0JSPS KAKENHI JP23K27568, JP23K18278, JP23K07229, and JP24K02230
6 · The paper itself

Abstract

purposeCornelia de Lange Syndrome (CdLS) is a rare genetic disorder that affects multiple organs, including the eyes. Ophthalmological findings in individuals with CdLS can vary, as occurs with certain features commonly associated with the syndrome, whose presence and severity can differ among patients. In this exploratory cross-sectional study, we aimed to report the ophthalmological phenotypes in a Brazilian CdLS cohort and evaluated possible genotype-phenotype associations.

methodsSixteen individuals with Cornelia de Lange Syndrome participated in this study. Only patients who had pathogenic or likely pathogenic variants in the NIPBL gene were included. Ophthalmological exams were conducted to investigate alterations in CdLS patients according to tolerance. The ophthalmic assessment comprised measurement of facial distances, ectoscopy, visual acuity, pupillary reaction, extrinsic ocular motility, slit lamp exam, tonometry, refraction under cycloplegia, and dilated fundus exam.

resultsOcular anomalies were identified in all CdLS patients, including abnormalities of the eyebrows, eyelashes, palpebral fissures, and anterior and posterior segments, as well as refractive errors, strabismus, and nystagmus. Although some phenotypes were exclusively present in patients with specific NIPBL variant types, no statistical significance was identified.

conclusionsThe ophthalmological findings in patients with CdLS are diverse and often significantly impact vision and quality of life. We recommend regular ophthalmological exams from the time of diagnosis to enable detection of treatable eye conditions, including refractive errors, ptosis, dry eyes, and strabismus, as early detection is essential for appropriate interventions and the prevention of long-term visual complications.

Indexed as

Cell Cycle ProteinsDe Lange SyndromeAdolescentAdultBrazilChildChild, PreschoolCross-Sectional StudiesFemaleHumansMalePhenotypeVisual AcuityYoung AdultCell Cycle ProteinsNIPBL protein, humanCornelia de lange syndromeEye abnormalitiesNIPBL gene variantOphthalmological findings

Identifiers

PMID41088053
PMCPMC12522856

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.