Article
Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype.
The British journal of ophthalmology - 1 Sept 1994
De Becker I, Riddell D C, Dooley J M, Tremblay F
Abstract excerpt
Fifteen consecutive patients with the Duchenne muscular dystrophy (DMD) phenotype were studied. Each patient was asked to undergo an ophthalmic examination, an electroretinogram (ERG), and to donate a blood sample for molecular diagnosis. All 15 patients had a normal ophthalmic examination. Elect...
Topics
- Adolescent
- Adult
- Child, Preschool
- Electroretinography
- Gene Deletion
- Humans
- Male
- Muscular Dystrophies
- Phenotype