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Spinal muscular atrophy: Diagnosis and management in a new therapeutic era
Author(s) -
Arnold W. David,
Kassar Darine,
Kissel John T.
Publication year - 2015
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.24497
Subject(s) - smn1 , spinal muscular atrophy , sma* , motor neuron , medicine , denervation , muscle biopsy , atrophy , electromyography , neuroscience , bioinformatics , pathology , physical medicine and rehabilitation , biology , biopsy , disease , computer science , algorithm
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. Muscle Nerve 51 : 157–167, 2015