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RETINAL DYSTROPHY IN A PATIENT WITH MCARDLE DISEASE.
Retinal Cases & Brief Reports 2018 August 2
PURPOSE: To report a case of pattern dystrophy in a patient with McArdle disease, a rare autosomal recessive disorder of glycogen metabolism.
METHODS: Case report.
RESULTS: A 29-year-old woman with a history of muscle biopsy-confirmed McArdle disease presented with fundus findings consistent with pattern dystrophy. Multimodal imaging, including optical coherence tomography and fundus autofluorescence, was performed.
CONCLUSION: To our knowledge, this is the third reported case of pattern dystrophy in a patient with McArdle disease.
METHODS: Case report.
RESULTS: A 29-year-old woman with a history of muscle biopsy-confirmed McArdle disease presented with fundus findings consistent with pattern dystrophy. Multimodal imaging, including optical coherence tomography and fundus autofluorescence, was performed.
CONCLUSION: To our knowledge, this is the third reported case of pattern dystrophy in a patient with McArdle disease.
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