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| LETTER TO THE EDITOR |
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| Year : 2013 | Volume
: 61
| Issue : 3 | Page : 133-135 |
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Retinitis pigmentosa associated with ectopia lentis in a patient with Marfan syndrome
Jifeng Yu1, Li Liang2, Yuqin Wen3, Yifei Huang1
1 Department of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, China
2 Department of Surgery, Chinese PLA General Hospital, Beijing 100853, China
3 Center of Anesthesia and Operation, Chinese PLA General Hospital, Beijing 100853, China
| Date of Web Publication | 21-Mar-2013 |
Correspondence Address:
Yifei Huang
Department of Ophthalmology, Chinese PLA General Hospital, 28 Fuxing Road, Haidian District, Beijing 100853
China
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0301-4738.109387
How to cite this article:
Yu J, Liang L, Wen Y, Huang Y. Retinitis pigmentosa associated with ectopia lentis in a patient with Marfan syndrome. Indian J Ophthalmol 2013;61:133-5 |
Dear Editor,
A 32-year-old, 6.2-foot man presented with complaints of defective vision since early childhood and a history of defective night vision. His father died of an unknown cause when he was 5 years old. The patient had visible arachnodactyly and hyperextensible joints [Figure 1], but this did not affect his life. Ocular examination revealed that both lenses were dislocated superiorly. Punctate anterior and posterior "snowflake" lens opacities resembled a complicated cataract [Figure 2]. Best-corrected visual acuities (BCVA) were 20/400 (-2.25), right, and 20/250 (-4.00), left, respectively. The anterior chamber was normal for both eyes. Intraocular pressures were 20 and 18 mmHg, respectively. We could not see the fundus clearly before the cataract surgery. Electroretinography (ERG) findings showed a barely detectable rod b-wave [Figure 3]. The amplitudes of a- and b-waves in the mixed cone-rod signal were reduced, and the cone response was delayed, suggesting a diagnosis of retinitis pigmentosa (RP). Marfan syndrome was confirmed through his tall height, arachnodactyly, hyperextensible joints and echocardiography [Figure 4]. Phacoemusification and anterior vitrectomy were performed on both eyes. Intraocular lens (IOL) was not implanted the first time. After the surgery, fundus photograph showed "bone-spicule formation" in both eyes [Figure 5]. BCVA were 20/50 (+10.00), right, and 20/25 (+12.50), left, respectively. Scleral fixated IOL were implanted 3 months later in order to improve the patient's quality of life. BCVA was 20/60 right and 20/50 left after the surgery. | Figure 1: The patient was visible arachnodactyly and hyperextensible joints
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 | Figure 2: Slit lamp photograph. Ectopia lentis is present in the right (a) and left (b) eyes
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 | Figure 3: ERG findings showed a barely detectable rod b-wave. The amplitudes of a- and b-waves in the mixed cone-rod signal were reduced, and the cone response was delayed
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 | Figure 4: Echocardiography findings. (a) The aortic sinus was widened; (b) the aortic root was seen as a fusiform expansion and (c and d) a small quantity of aortic regurgitation
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 | Figure 5: (a) Fundus photograph of the right (a) and left (b) eyes. Bone-spicule pigmentation is present in the entire retina; (b) Fundus photograph of the right (a) and left (b) eyes. Bone-spicule pigmentation is present in the entire retina
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About 50% of the patients with Marfan syndrome are diagnosed by ophthalmologists. The presence of ectopia lentis (EL) is considered a major criterion for the diagnosis of Marfan syndrome in nosology, which unequivocally diagnoses or excludes Marfan syndrome in 86% of the cases. [1]
Although the link between RP and EL has been reported before, [2],[3],[4] systemic symptoms have not been reported. The only complaint of the current case was defective vision, and EL was found during the eye examination. Considering his 6.2-foot height (taller than average Chinese man), arachnodactyly, hyperextensible joints and echocardiography, a systemic examination was performed and Marfan syndrome was then confirmed. These results suggest that a systemic examination may be necessary in tall subjects with poor vision.
To the best of our knowledge, this is the first report of bilateral spontaneous EL associated with RP in a patient with Marfan syndrome.
| References | |  |
| 1. | Dean JC. Marfan syndrome: Clinical diagnosis and management. Eur J Hum Genet 2007;15:724-33.  [ PUBMED] |
| 2. | Eid TM. Retinitis pigmentosa associated with ectopia lentis and acute angle-closure glaucoma. Can J Ophthalmol 2008;43:726-7. [ PUBMED] |
| 3. | Kwon YA, Bae SH, Sohn YH. Bilateral spontaneous anterior lens dislocation in a retinitis pigmentosa patient. Korean J Ophthalmol 2007;21:124-6. [ PUBMED] |
| 4. | Sato H, Wada Y, Abe T, Kawamura M, Wakusawa R, Tamai M. Retinitis pigmentosa associated with ectopia lentis. Arch Ophthalmol 2002;120:852-4. [ PUBMED] |
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]
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