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DOI 10.3109/13816810.2014.886268

Медицинская библиотека · Ophthalmic genetics · 2014

Visual Impairment in Pseudoxanthoma Elasticum: A Survey of 40 Patients.

Orssaud Christophe, Roche Olivier, Dufier Jean-Louis, Germain Dominique P

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Аннотация

BACKGROUND

Pseudoxanthoma elasticum is an inherited disorder of connective tissue characterized, among other symptoms, by impaired vision.

OBJECTIVE

To evaluate the nature and age of onset of ophthalmologic manifestations in pseudoxanthoma elasticum.

PATIENTS AND

METHODS

Forty consecutive patients affected with pseudoxanthoma elasticum underwent measurements of their refractive error and visual acuity, together with slit-lamp examination.

RESULTS

The mean age of the patients (8 M, 32 F) was 43.35 years. Fifty-seven eyes (33 patients, mean age: 40.75 years) had a BCVA >20/50 whereas 23 eyes in 16 patients (mean age: 53.31 years) had ≤20/50. Seven patients (17.50%), all but one over 52 years old, were visually disabled. BCVA ≤20/50 in at least one eye was observed in 73.33% of patients of 52 years old or older and in 20.00% of patients younger than 52, respectively. Angioid streaks were observed in 75 eyes (93.75%) and extended toward the macula in 51 eyes from 29 patients. Macular involvement was observed for the first time at a mean age of 44.28 years. Neovascularization was observed in 28 eyes (17 patients; mean age: 51.70 years), all with poor BCVA.

CONCLUSION

Macular choroidal neovascularization is frequent in pseudoxanthoma elasticum, and accounts for the poor ophthalmologic natural history of the disease. Patients should be advised to self-monitor their visual acuity using the Amsler grid. The frequency of choroidal neovascularization appears age-dependent, suggesting that bi-yearly fundus examination is appropriate in young patients whereas patients older than 40 should be examined twice a year.

Для цитирования: Orssaud Christophe, Roche Olivier, Dufier Jean-Louis, Germain Dominique P. Visual Impairment in Pseudoxanthoma Elasticum: A Survey of 40 Patients.. Ophthalmic genetics. 2014. DOI: 10.3109/13816810.2014.886268.

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