Codi QR

Review of therapeutic options for spinal muscular atrophy

Spinal Muscular Atrophy (SMA) is uncommon genetic (autosomal recessive) disease that deteriorates neuromuscular function of the affected person's body by causing lower motor neuron damage, progress in muscle atrophy and in advanced cases leads to paralysis of muscles. Mainly skeletal and respiratory...

Descripció completa

Guardat en:
Autors principals: Singh Arun, Jain Monica, Kapadia Rupa, Mahawar-Dhirendra Kumar, Kakkar Shivankan, Dadhich Jaya, Chandel-Ritesh Kumar
Format: Artigo
Idioma:Inglês
Publicat: Medical Society of the Republic of Srpska, Banja Luka, University of Banja Luka. Faculty of Medicine 2021-01-01
Col·lecció:Scripta Medica
Matèries:
spinal muscular atrophy
smn-1
rare disease frequency
therapeutic approaches
risdiplam
nusinersen
onasemnogene abeparvovec
Accés en línia:https://scindeks-clanci.ceon.rs/data/pdf/2490-3329/2021/2490-33292102151S.pdf
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars