Spinal muscular atrophy: diagnosis and management in a new therapeutic era.
Muscle Nerve
; 51(2): 157-67, 2015 Feb.
Article
en En
| MEDLINE
| ID: mdl-25346245
ABSTRACT
Spinal muscular atrophy (SMA) describes a group of disorders associated with spinal motor neuron loss. In this review we provide an update regarding the most common form of SMA, proximal or 5q-SMA, and discuss the contemporary approach to diagnosis and treatment. Electromyography and muscle biopsy features of denervation were once the basis for diagnosis, but molecular testing for homozygous deletion or mutation of the SMN1 gene allows efficient and specific diagnosis. In combination with loss of SMN1, patients retain variable numbers of copies of a second similar gene, SMN2, which produces reduced levels of the survival motor neuron (SMN) protein that are insufficient for normal motor neuron function. Despite the fact that understanding of how ubiquitous reduction of SMN protein leads to motor neuron loss remains incomplete, several promising therapeutics are now being tested in early-phase clinical trials.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Asunto principal:
Atrofia Muscular Espinal
Tipo de estudio:
Diagnostic_studies
Límite:
Humans
Idioma:
En
Revista:
Muscle Nerve
Año:
2015
Tipo del documento:
Article
País de afiliación:
Estados Unidos