Cone dystrophy with supernormal rod response – A rare case report
Cone dystrophy with supernormal rod response (CDSRR), also known as potassium channel subfamily V, member 2 (KCNV2) retinopathy, is a rare autosomal recessive cone rod dystrophy, which derives its name from its characteristic full-field electroretinography (ERG) features and the causative gene mutat...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Wolters Kluwer Medknow Publications
2024-01-01
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| Σειρά: | Indian Journal of Ophthalmology. Case Reports |
| Θέματα: | |
| Διαθέσιμο Online: | https://journals.lww.com/10.4103/IJO.IJO_363_23 |
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