- 영문명
- 발행기관
- 대한안과학회
- 저자명
- Jae Lim Chung Sun Woong Kim Hyun Kim Tae-im Kim Hyung Keun Lee Eung Kweon Kim
- 간행물 정보
- 『The Korean Journal of Ophthalmology』Vol.21 No.4, 255~260쪽, 전체 6쪽
- 주제분류
- 의약학 > 의학일반
- 파일형태
- 발행일자
- 2007.12.30
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국문 초록
영문 초록
Purpose: To present a case of Weill-Marchesani syndrome with corneal endothelial dysfunction due to anterior dislocation of a spherophakic lens and corneolenticular contact.
Methods: A 17-year-old woman presented with high myopia and progressive visual disturbance. She was of short stature and had brachydactyly. Her initial Snellen best corrected visual acuity (BCVA) was 20/50 (-sph 20.50 -cyl 3.00 Ax 180) in her right eye and 20/40 (-sph 16.00 -cyl 6.00 Ax 30) in her left eye. Slit lamp examination revealed a dislocated spherophakic lens touching corenal endothelium. A microspherophakic lens, hypoplastic ciliary body, and elongated zonules were confirmed on rotating Scheimpflug camera (PentacamⓇ) and on ultrasound biomicroscopy. Specular microscopy showed corneal endothealial dysfunction. Systemic evaluation was performed, and chromosomal study showed 46, XX, inv(15) (q13qter). The patient was diagnosed with Weill-Marchesani syndrome.
Results: Due to impending corneal decompensation, phacoemulsification and suture fixation of the
intraocular lens were performed. The operation and postoperative course were uneventful. Three months postoperatively, the visual acuity was 20/30 (OD) and 20/40 (OS) without correction, and BCVA was 20/20
(+sph 0.50 -cyl 2.00 Ax 160 : OD) and 20/25 (+sph 1.50 -cyl 3.00 Ax 30 : OS). During the follow-up period,
increased corneal endothelial counts, hexagonality, and decreased corneal thickness were achieved.
Conclusions: In Weill-Marchesani syndrome with a chromosomal anomaly, a dislocated spherophakic lens
may cause severe corneal endothelial dysfunction due to corneolenticular contact, and prompt lensectomy
is important to prevent such complications.
목차
Case Report
Discussion
References
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- Korean Journal of Ophthalmology Vol. 21 No. 4 목차
- A Case of Weill-Marchesani Syndrome with Inversion of Chromosome 15
- Instructions to Authors
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