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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/10860
Title: Duchenne muscular dystrophy and limb-girdle muscular dystrophy: clinical cases
Authors: Bejan, Nadejda
Keywords: Muscular dystrophies (MD);Duchenne muscular dystrophy (DMD);limb-girdle muscular dystrophies (LGMDs)
Issue Date: 2018
Publisher: MedEspera
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.
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.
URI: https://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf
http://repository.usmf.md/handle/20.500.12710/10860
Appears in Collections:MedEspera 2018

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