Duchenne muscular dystrophy and limb-girdle muscular dystrophy: clinical cases

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