| DC Field | Value | Language |
|---|
| dc.contributor.author | Bejan, Nadejda | - |
| dc.date.accessioned | 2020-07-02T15:08:04Z | - |
| dc.date.available | 2020-07-02T15:08:04Z | - |
| dc.date.issued | 2018 | - |
| dc.identifier.citation | BEJAN, Nadejda. Duchenne muscular dystrophy and limb-girdle muscular dystrophy: clinical cases. In: MedEspera: the 7th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2018, p. 31. | en_US |
| dc.identifier.uri | https://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf | - |
| dc.identifier.uri | http://repository.usmf.md/handle/20.500.12710/10860 | - |
| dc.description | Nicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldova | en_US |
| dc.description.abstract | Background : Muscular dystrophies (MD) represent a large group of genetic disorders that are
manifested by progressive increase of muscle weakness. Duchenne muscular dystrophy (DMD)
is an X-linked disorder and limb-girdle muscular dystrophies (LGMDs) include over thirty
subtypes, that are classified in autosomal dominant (1A-1H) and recessive (2A-2W). Our aims
was to highlight the clinical and genetic aspects in MD by reporting two clinical cases with the
aim of improving the early diagnosis. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | MedEspera | en_US |
| dc.subject | Muscular dystrophies (MD) | en_US |
| dc.subject | Duchenne muscular dystrophy (DMD) | en_US |
| dc.subject | limb-girdle muscular dystrophies (LGMDs) | en_US |
| dc.title | Duchenne muscular dystrophy and limb-girdle muscular dystrophy: clinical cases | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | MedEspera 2018
|
