Phenotype of Coats disease in females

被引:3
作者
Daruich, Alejandra [1 ,2 ]
Munier, Francis L. [3 ]
机构
[1] Univ Paris, Hop Necker Enfants Malad, AP HP, Ophthalmol Dept, Paris, France
[2] INSERM, Ctr Rech Cordeliers, Team 17, Paris, France
[3] Univ Lausanne, Jules Gonin Eye Hosp, Fdn Asile Aveugles, Ophthalmol Dept, Lausanne, Switzerland
关键词
Retina; Child health (paediatrics); CLASSIFICATION; INACTIVATION; MANAGEMENT; FEATURES; OUTCOMES; NORRIN; GENE; AGE;
D O I
10.1136/bmjophth-2021-000883
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objective To determine whether the clinical presentation of Coats disease differs between males and females. Methods and analysis Records of patients diagnosed with Coats disease at a single institution were retrospectively reviewed. Demographic data, main reason for initial consultation, comprehensive ocular examination at diagnosis and modalities of treatments during the follow-up were recorded. Results Records from 114 patients with Coats disease were analysed. Ninety-eight patients (86%) were male and 16 (14%) female. Mean age at diagnosis was 6.2 years +/- 6.1 in males and 7.4 years +/- 4.7 in females. The main initial reason for consultation was strabismus in males and decreased visual acuity in females. Stage severity at diagnosis was similar in the two groups with half of the patients presenting with stage 2B2 or lower. The extension of peripheral retinal telangiectasia was also similar (mean: 6.2 +/- 3.4 and 5.8 +/- 4.0, respectively), as was the extension of intraretinal exudation (mean: 5.0 +/- 4.5 and 5.8 +/- 4.4) and the frequency of a subfoveal nodule at diagnosis (40% vs 30%, respectively). There was no distinction between the number of laser photocoagulation or cryotherapy sessions required for both groups during the follow-up. Conclusions Coats disease presentation does not differ between genders despite being much rarer in females. We propose a pathogenic mechanism accounting for the gender-dependent incidence combined with gender-independent expressivity of Coats disease.
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页数:3
相关论文
共 15 条
[1]   Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis [J].
Black, GCM ;
Perveen, R ;
Bonshek, R ;
Cahill, M ;
Clayton-Smith, J ;
Lloyd, IC ;
McLeod, D .
HUMAN MOLECULAR GENETICS, 1999, 8 (11) :2031-2035
[2]   X-inactivation profile reveals extensive variability in X-linked gene expression in females [J].
Carrel, L ;
Willard, HF .
NATURE, 2005, 434 (7031) :400-404
[3]  
CIDECIYAN AV, 1994, INVEST OPHTH VIS SCI, V35, P3812
[4]  
Coats G., 1908, Roy Lond Ophthalmol Hosp Rep, V17, P440
[5]   Coats Disease: Clinical Features and Outcomes by Age Category in 351 Cases [J].
Dalvin, Lauren A. ;
Udyaver, Sanika ;
Lim, Li-Anne S. ;
Mazloumi, Mehdi ;
Atalay, Hatice T. ;
Khoo, Chloe T. L. ;
Shields, Carol L. .
JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS, 2019, 56 (05) :288-+
[6]   YOUNGER AGE AT PRESENTATION IN CHILDREN WITH COATS DISEASE IS ASSOCIATED WITH MORE ADVANCED STAGE AND WORSE VISUAL PROGNOSIS A Retrospective Study [J].
Daruich, Alejandra ;
Matet, Alexandre ;
Munier, Francis L. .
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2018, 38 (11) :2239-2246
[7]   SUBFOVEAL NODULE IN COATS' DISEASE Toward an Updated Classification Predicting Visual Prognosis [J].
Daruich, Alejandra L. ;
Moulin, Alexandre P. ;
Tran, Hoai V. ;
Matet, Alexandre ;
Munier, Francis L. .
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2017, 37 (08) :1591-1598
[8]   The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies [J].
De Silva, Samantha R. ;
Arno, Gavin ;
Robson, Anthony G. ;
Fakin, Ana ;
Pontikos, Nikolas ;
Mohamed, Moin D. ;
Bird, Alan C. ;
Moore, Anthony T. ;
Michaelides, Michel ;
Webster, Andrew R. ;
Mahroo, Omar A. .
PROGRESS IN RETINAL AND EYE RESEARCH, 2021, 82
[9]   X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa [J].
Fahim, Abigail T. ;
Sullivan, Lori S. ;
Bowne, Sara J. ;
Jones, Kaylie D. ;
Wheaton, Dianna K. H. ;
Khan, Naheed W. ;
Heckenlively, John R. ;
Jayasundera, K. Thiran ;
Branham, Kari H. ;
Andrews, Chris A. ;
Othman, Mohammad, I ;
Karoukis, Athanasios J. ;
Birch, David G. ;
Daiger, Stephen P. .
OPHTHALMOLOGY RETINA, 2020, 4 (05) :510-520
[10]   The Role of X-Chromosome Inactivation in Retinal Development and Disease [J].
Fahim, Abigail T. ;
Daiger, Stephen P. .
RETINAL DEGENERATIVE DISEASES: MECHANISMS AND EXPERIMENTAL THERAPY, 2016, 854 :325-331