myotonic dystrophy type 1;
cataract;
eyelid ptosis;
intraocular pressure;
Motor Function Measure scale;
Portuguese version;
MOTOR FUNCTION;
CTG REPEAT;
CATARACT;
GENE;
EXPRESSION;
SIX5;
MICE;
D O I:
10.1590/0004-282X20150218
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
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.
机构:
Hacettepe Univ, Fac Med, Dept Pediat Neurol, Ankara, Turkey
Gazi Univ, Fac Med, Dept Pediat Neurol, Ankara, TurkeyHacettepe Univ, Fac Med, Dept Pediat Neurol, Ankara, Turkey
Esra, Serdaroglu
Ceren, Gunbey
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机构:
Hacettepe Univ, Fac Med, Dept Pediat Neurol, Ankara, TurkeyHacettepe Univ, Fac Med, Dept Pediat Neurol, Ankara, Turkey
Ceren, Gunbey
Banu, Anlar
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机构:
Hacettepe Univ, Fac Med, Dept Pediat Neurol, Ankara, TurkeyHacettepe Univ, Fac Med, Dept Pediat Neurol, Ankara, Turkey