Myotonic dystrophy-2: Unusual phenotype due to a small CCTG-expansion
Myotonic dystrophy type 2 (MD2) is a multisystem disease, predominantly affecting the proximal limb muscles, eyes, endocrine organs, heart and intestines. Longterm asymptomatic creatine kinase (hyper-CKemia) of more than 20 years duration, in association with hyperlipidemia and diabetes, as a manife...
| Published in: | Balkan Journal of Medical Genetics |
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| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Sciendo
2018-12-01
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| Subjects: | |
| Online Access: | https://doi.org/10.2478/bjmg-2018-0024 |
