Myotonic Dystrophy Type 1 Associating Sensitive Polyneuropathy: a Case Report
Introduction: Myotonic dystrophy (DM) type 1 is a genetic disorder, caused by a trinucleotide CTG repeat expansion in the DMPK gene on chromosome 19. The skeletal muscle is the most severely affected organ, patients clinically presenting weakness and myotonia. Additionally, it may affect other organ...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Media Med Publicis
2020-03-01
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| Series: | Modern Medicine |
| Subjects: | |
| Online Access: | https://medicinamoderna.ro/wp-content/uploads/2020/03/RMM_art-9.pdf |