Artículos de revistas
Myotonic Dystrophy Type 1: Frequency Of Ophthalmologic Findings
Registro en:
Arquivos De Neuro-psiquiatria. Assoc Arquivos Neuro- Psiquiatria, v. 74, p. 183 - 188, 2016.
0004-282X
1678-4227
WOS:000374191900002
10.1590/0004-282X20150218
Autor
Ikeda
Karin Suzete; Iwabe-Marchese
Cristina; Franca
Marcondes Cavalcante
Jr.; Nucci
Anamarli; de Carvalho
Keila Monteiro
Institución
Resumen
The purpose of the study was to evaluate the frequency of ophthalmologic abnormalities in a cohort of myotonic dystrophy type 1 (DM1) patients and to correlate them with motor function. We reviewed the pathophysiology of cataract and low intraocular pressure (IOP). Method: Patients were included after clinical and laboratory diagnosis and after signed informed consent. They were evaluated by Motor Function Measure scale, Portuguese version (MFM-P) and ophthalmic protocol. Results: We evaluated 42 patients aged 17 to 64 years (mean 40.7 +/- 12.5), 22 of which were men. IOP (n = 41) was reduced in all but one. We found cataract or positivity for surgery in 38 (90.48%) and ptosis in 23 (54.76%). These signs but not IOP were significantly correlated with severity of motor dysfunction. Abnormalities in ocular motility and stereopsis were observed. Conclusion: Cataract and ptosis are frequent in DM1 and associated to motor dysfunction. Reduced IOP is also common, but appears not to be related with motor impairment. 74 3 183 188