Ocular Manifestations and Biometrics in Marfan's Syndrome from Eastern Nepal.

Marfan’s syndrome corneal astigmatism ectopia lentis flattened cornea ocular biometry

Journal

Clinical ophthalmology (Auckland, N.Z.)
ISSN: 1177-5467
Titre abrégé: Clin Ophthalmol
Pays: New Zealand
ID NLM: 101321512

Informations de publication

Date de publication:
2020
Historique:
received: 03 07 2020
accepted: 10 08 2020
entrez: 9 9 2020
pubmed: 10 9 2020
medline: 10 9 2020
Statut: epublish

Résumé

To evaluate the ocular characteristics of Marfan's syndrome (MFS) fulfilling the revised Ghent-2 nosology in Eastern Nepal. A hospital-based observational and cross-sectional study was conducted. Ocular manifestations and biometrics were incorporated. Patients were subdivided into adults (16 years or older) and children (5-15 years). Ocular biometric parameters consisted of values of refractive error, keratometry readings, anterior chamber depth (ACD), central corneal thickness (CCT), lens thickness (LT) and axial length (AL). A total of 34 eyes of 17 patients with MFS were included, where 32 eyes were phakic. Mean age of the study participants was 14.5 ± 9.1 years. The mean best corrected visual acuity (BCVA) of phakic eyes was 0.99 ± 0.82 LogMAR. Myopia greater than -3 diopters (D) was present in 28/34 (82.35%) eyes. The average spherical equivalent was -12.34 ± 8.85 D. Ectopia lentis (EL) was present in 24/32 (75%) eyes where superonasal was the most common subluxation in 10/24 (41.7%) eyes. AL was longer in adults 26.54 ± 4.42 mm compared to 25.21 ± 1.93 mm in children. Likewise, LT in adults was 4.9 ± 0.70 mm and 4.40 ± 0.59 mm in pediatric participants. Flat corneas were noted in both the groups with an average of 41.53 ± 2.21 D. The mean CCT and ACD were 524.62 ± 21.74 μm and 3.64 ± 0.80 mm, respectively. There was a negative association between the AL and the average corneal curvature (K Myopia is the foremost ocular involvement with significant visual disability in MFS. Though, AL and corneal curvature are not included in the revised Ghent-2 nosology, we strongly recommend these parameters to be considered during ophthalmic evaluation in suspected and diagnosed cases of MFS in the absence of genetic testing.

Identifiants

pubmed: 32904572
doi: 10.2147/OPTH.S269364
pii: 269364
pmc: PMC7457576
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2463-2472

Informations de copyright

© 2020 Suwal et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

Références

Retina. 2002 Aug;22(4):423-8
pubmed: 12172108
Am J Ophthalmol. 2017 May;177:144-149
pubmed: 28257833
Acta Ophthalmol. 2015 Feb;93(1):46-53
pubmed: 24853997
Eur J Hum Genet. 2002 Nov;10(11):673-81
pubmed: 12404097
Acta Ophthalmol. 2013 Dec;91(8):751-5
pubmed: 23387925
J Med Genet. 1994 Jan;31(1):51-4
pubmed: 8151638
Acta Ophthalmol (Copenh). 1986 Oct;64(5):487-91
pubmed: 3492854
J Med Genet. 2006 Oct;43(10):769-87
pubmed: 16571647
Ophthalmic Physiol Opt. 1989 Jul;9(3):235-8
pubmed: 2622662
J Cataract Refract Surg. 2007 May;33(5):819-24
pubmed: 17466855
Am J Hum Genet. 2007 Sep;81(3):454-66
pubmed: 17701892
Can J Ophthalmol. 2016 Apr;51(2):113-8
pubmed: 27085269
J All India Ophthalmol Soc. 1966 Dec;14(6):262-3
pubmed: 5990447
N Engl J Med. 1979 Apr 5;300(14):772-7
pubmed: 370588
Trans Am Ophthalmol Soc. 1981;79:684-733
pubmed: 7043871
Acta Ophthalmol. 2014 Feb;92(1):e82-3
pubmed: 23786577
Am J Med Genet. 1996 Apr 24;62(4):417-26
pubmed: 8723076
Surv Ophthalmol. 2006 Nov-Dec;51(6):561-75
pubmed: 17134646
Acta Ophthalmol Scand. 2007 Jun;85(4):361-6
pubmed: 17286626
Am J Ophthalmol. 2008 Jun;145(6):997-1001
pubmed: 18378212
Eur J Hum Genet. 2009 Oct;17(10):1222-30
pubmed: 19293838
Ophthalmology. 2009 Jul;116(7):1343-8
pubmed: 19427698
Genomics. 1991 Feb;9(2):355-61
pubmed: 2004786
Acta Ophthalmol. 2012 Jun;90(4):375-9
pubmed: 21726424
Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1757-64
pubmed: 12036976
J Med Genet. 2010 Jul;47(7):476-85
pubmed: 20591885
PLoS One. 2017 Sep 20;12(9):e0183370
pubmed: 28931008
Eur J Hum Genet. 2007 Jul;15(7):724-33
pubmed: 17487218
Retina. 2003 Feb;23(1):24-9
pubmed: 12652227
Nature. 1991 Jul 25;352(6333):337-9
pubmed: 1852208
Am J Med Genet. 1988 Mar;29(3):581-94
pubmed: 3287925
Optom Vis Sci. 1994 Sep;71(9):573-9
pubmed: 7816428
Arch Ophthalmol. 1967 Sep;78(3):289-96
pubmed: 6040004
Acta Ophthalmol (Copenh). 1988 Jun;66(3):334-40
pubmed: 10994457
Int Ophthalmol Clin. 2001 Fall;41(4):235-40
pubmed: 11698751
Lancet. 2005 Dec 3;366(9501):1965-76
pubmed: 16325700
Trans Am Acad Ophthalmol Otolaryngol. 1967 Jan-Feb;71(1):18-38
pubmed: 4963574
J Cataract Refract Surg. 2012 Feb;38(2):309-14
pubmed: 22153358
Arch Ophthalmol. 1992 Apr;110(4):472-3
pubmed: 1562249
Am J Ophthalmol. 1973 Mar;75(3):405-20
pubmed: 4633235

Auteurs

Rinkal Suwal (R)

Department of Optometry, BP Eye Foundation, Hospital for Children, Eye, ENT and Rehabilitation Service (CHEERS), Bhaktapur, Nepal.

Simanta Khadka (S)

Department of Vitreo-Retina, Bharatpur Eye Hospital, Bharatpur, Chitwan, Nepal.

Purushottam Joshi (P)

Department of Vitreo-Retina, Mechi Eye Hospital, Birtamod, Jhapa, Nepal.

Classifications MeSH