Spinal Muscular Atrophy



The spinal muscular atrophies (SMAs) comprise a group of autosomal-recessive disorders characterized by progressive weakness of the lower motor neurons.

In the early 1890s, Werdnig and Hoffman described a disorder of progressive muscular weakness beginning in infancy that resulted in early death, though the age of death was variable. In pathologic terms, the disease was characterized by loss of anterior horn cells. The central role of lower motor neuron degeneration was confirmed in subsequent pathologic studies demonstrating a loss of anterior horn cells in the spinal cord and cranial nerve nuclei.[1]

Since then, several types of spinal muscular atrophies have been described based on age when accompanying clinical features appear. The most common types are acute infantile (SMA type I, or Werdnig-Hoffman disease), chronic infantile (SMA type II), chronic juvenile (SMA type III or Kugelberg-Welander disease), and adult onset (SMA type IV) forms.

The genetic defects associated with SMA types I-III are localized on chromosome 5q11.2-13.3.[2, 3, 4, 5]

Many classification systems have been proposed and include variants based on inheritance, clinical, and genetic criteria. Among these are the Emery[6] , Pearn[7] , and International SMA Consortium system[8] . The ISMAC system is most widely accepted and is used in this review.


In 1995, the spinal muscular atrophy disease-causing gene, termed the survival motor neuron (SMN), was discovered.[9] Each individual has 2 SMN genes, SMN1 and SMN2. More than 95% of patients with spinal muscular atrophy have a homozygous disruption in the SMN1 gene on chromosome 5q, caused by mutation, deletion, or rearrangement. However, all patients with spinal muscular atrophy retain at least 1 copy of SMN2, which generates only 10% of the amount of full-length SMN protein versus SMN1. This genomic organization provides a therapeutic pathway to promote SMN2, existing in all patients, to function like the missing SMN1 gene.[10]



United States

The spinal muscular atrophies are the second most common autosomal-recessive inherited disorders after cystic fibrosis. The acute infantile-onset SMA (type I) affects approximately 1 per 10,000 live births; the chronic forms (types II and III) affect 1 per 24,000 births. SMA types I and III each account for about one fourth of cases, whereas SMA type II is the largest group and accounts for one half of all cases.[11]


The incidence of spinal muscular atrophy is about 1 in 10,000 live births with a carrier frequency of approximately 1 in 50.[7, 12, 13]


The mortality and/or morbidity rates of spinal muscular atrophy are inversely correlated with the age at onset. High death rates are associated with early onset disease. In patients with SMA type I, the median survival is 7 months, with a mortality rate of 95% by age 18 months.


Male individuals are most frequently affected, especially with the early-onset forms of spinal muscular atrophy, ie, types I and II.[14]


The ISMAC classification system is based on the age of onset.[8] See Background, History, and Physical for a review of the existing classification systems and a brief discussion of their relevancy to the role of age in spinal muscular atrophies.

According to the ISMAC system, the age of onset for spinal muscular atrophies is as follows:


The diagnosis of spinal muscular atrophies includes the following a detailed clinical history. Obtaining a complete family history facilitates genetic counseling.

Patients with spinal muscular atrophy present with weakness and muscle wasting in the limbs, respiratory, and bulbar or brainstem muscles. They have no evidence of cerebral or other CNS dysfunction. Patients with spinal muscular atrophy often have above-average intelligence quotients (IQs) and demonstrate high degrees of intelligence.

The clinical manifestations of each particular form of spinal muscular atrophy are discussed:[15, 2, 16, 17, 18]

SMA type I - Acute infantile or Werdnig-Hoffman disease

Patients present before 6 months of age, with 95% of patients having signs and symptoms by 3 months. They have severe, progressive muscle weakness and flaccid or reduced muscle tone (hypotonia). Bulbar dysfunction includes poor suck ability, reduced swallowing, and respiratory failure. Patients have no involvement of the extraocular muscles, and facial weakness is often minimal or absent. They have no evidence of cerebral involvement, and infants appear alert.

Reports of impaired fetal movements are observed in 30% of cases, and 60% of infants with SMA type I are floppy babies at birth. Prolonged cyanosis may be noted at delivery. In some instances, the disease can cause fulminant weakness in the first few days of life. Such severe weakness and early bulbar dysfunction are associated with short life expectancy, with a mean survival of 5.9 months. In 95% of cases, infants die from complications of the disease by 18 months.

SMA type II - Chronic infantile form

This is the most common form of spinal muscular atrophy, and some experts believe that SMA type II may overlap types I and III.

Most children present between the ages of 6 and 18 months.

The most common manifestation that parents and physicians note is developmental motor delay. Infants with SMA type II often have difficulties with sitting independently or failure to stand by 1 year of age.

An unusual feature of the disease is a postural tremor affecting the fingers. This is thought to be related to fasciculations in the skeletal muscles.

Pseudohypertrophy of the gastrocnemius muscle, musculoskeletal deformities, and respiratory failure can occur.

The lifespan of patients with SMA type II varies from 2 years to the third decade of life. Respiratory infections account for most deaths.

SMA type III - Chronic juvenile or Kugelberg-Welander syndrome

This is a mild form of autosomal recessive spinal muscular atrophy that appears after age 18 months.

SMA type III is characterized by slowly progressive proximal weakness. Most children with SMA III can stand and walk but have trouble with motor skills, such as going up and down stairs.

Bulbar dysfunction occurs late in the disease.

Patients may show evidence of pseudohypertrophy, as in patients with SMA type II.

The disease progresses slowly, and the overall course is mild. Many patients have normal life expectancies.

SMA type IV - Adult-onset form

Onset is typically in the mid 30s.

In many ways, the disease mimics the symptoms of type III.

Overall, the course of the disease is benign, and patients have a normal life expectancy.


Patients with disease of the lower motor neurons present with flaccid weakness, hypotonia, decreased or absent deep tendon reflexes, fasciculations, and muscle atrophy.

SMA type I - Acute infantile or Werdnig-Hoffman disease

Diffuse muscle weakness and hypotonia can be demonstrated with a variety of bedside maneuvers, including the traction response, vertical suspension, and horizontal suspension tests.

In general, infants with SMA type I cannot hold their heads up when pulled to the sitting position, and they will slip through the examiner's hands when held vertically. They lay limp in the physician's hand when held under the abdomen and facing down.

Weakness is greater in proximal than distal muscles and may mimic muscle disease (myopathy).

Findings on sensory examination are normal. Deep tendon reflexes are absent, as are long-tract signs and sphincteral abnormalities.

Arthrogryposis, or deformities of the limbs and joints at birth, can be observed and results from in utero hypotonia. Skeletal deformities (scoliosis) may be present.

In the infant or newborn, fasciculations are often restricted to the tongue, but tongue fasciculations can be difficult to distinguish from normal random movements unless atrophy is also present.

SMA type II - Chronic infantile form

Infants cannot get to a sitting position on their own, though they may stay upright if placed in that position.

As with SMA type I, SMA type II cause notable, symmetric proximal weakness, hypotonia, and fasciculations.

Findings on sensory examination are normal, and long-tract signs are absent. When the patient's hands are held out, a characteristic fine postural tremor may be observed.

SMA type III - Chronic juvenile or Kugelberg-Welander syndrome

Children can ambulate, but they have proximal muscle weakness and various degrees of muscle hypotonia and wasting.

The lower extremities are often more severely affected than the upper extremities.

SMA type IV - Adult-onset form

Patients are similar to those with SMA type III in presentation and clinical findings, though the overall degree of motor weakness is less severe in type IV than in type III.

Spinal muscular atrophy variants:

See the list below:


In 1995, the SMN gene, responsible for SMA types I-III, was mapped to the long arm of chromosome 5. (See Pathophysiology.)

Two copies of the SMN gene have been identified on the 5q arm: a telomeric SMN gene (SMNt, or SMN1) and a centromeric SMN gene (SMNc, or SMN2). These 2 genes are nearly identical except for base-pair changes in exons 7 and 8. About 95% of all cases of SMA involve a homozygous deletion of the SMN1 gene.[31]

Expression of SMN1 produces the full-length SMN protein. In contrast, expression of SMN2 produces a truncated version of the SMN protein that is missing the 16 amino acids from the carboxy terminus. This truncated protein results from a base-pair switch in exon 7 of the SMN2 gene. This switch leads to alternative splicing of SMN2 mRNA, with removal of the exon 7 sequence. About 70-80% of the gene product is in the form of this truncated protein. Only about 10-25% of the protein produced is the full-length functioning form.[31]

Deletions or mutations in the SMN1 gene substantially decrease expression of the SMN protein. Expression of SMN2 alone does not appear to produce sufficient amounts of SMN protein to permit normal mRNA processing in the lower motor neurons. A correlation between SMN2 copy number and disease phenotype has been proposed, with increased copy associated with milder disease.[32] Additionally, low SMN protein levels are associated with more severe disease forms.[33] Inefficient or abnormal mRNA processing appears to have a toxic effect on the lower motor neurons and results in cellular degeneration.[34]

SMN protein is part of a multimeric protein complex that plays a critical role in the assembly of snRNPs. These snRNPs are essential for early pre-mRNA splicing. The hypothesis is that impaired or reduced formation of snRNPs impairs mRNA splicing, with a toxic effect on normal cellular function. Why this mutation results in such selective degeneration of lower motor neurons is unclear, though the SMN protein is expressed in many types of neurons and organ systems.[35]

Neuronal apoptosis inhibitory protein (AIP), NAIP, gene was also identified in 1995. Homozygous deletions of this gene are found in 45% of patients with SMA type I and in 18% of patients with SMA types II or III. This gene belongs to a class of highly conserved AIPs that help to regulate programmed cell death. Deletion of this gene appears to be associated with severe phenotypes of SMA.[36]

Mutations in BFT2p44 have been found in 15% of patients with SMA.[37]

Laboratory Studies

Laboratory testing

The creatine kinase (CK) level is typically normal in SMA type I and normal or slightly elevated in the other types.

CSF findings are normal.

Genetic testing

Both prenatal and postnatal tests are now commercially available.

Homozygous SMN1 gene deletion is 95% sensitive and nearly 100% specific for the diagnosis of SMA. In patients with suspected disease and no gene deletion, SMN1 copy testing with sequencing of coding regions of SMN1 copy (if present) is suggested.[38]  Molecular testing for homozygous deletion or mutation of the SMN1 gene allows efficient and specific diagnosis.[39]

The 1992 ISMAC found that the accuracy of prenatal prediction by means of chorionic villi sampling and amniocentesis was 88-99%.

Caution should be exercised when prenatal prediction is done in the presence of atypical features (see SMA variants in Physical) because these clinical variations may represent other pathogenic processes.


Other Tests

Most cases spare the cardiac system, and ECGs are normal.[40]

Electrophysiologic studies are useful in differentiating the spinal muscular atrophies from other neurogenic and myopathic diseases.[41, 42] With the exception of Kennedy and Davidenkow syndromes, sensory nerve conduction is normal in spinal muscular atrophy.

Compound motor action potentials (CMAPs) are low normal or reduced, depending on the severity of disease. In chronically weak muscles, CMAPs may be in the near-normal because of reinnervation and collateral sprouting. Motor velocities are normal. Modest slowing of motor conduction, when present, may accompany severe motor axon loss because of the loss of the fastest-conducting motor fibers.

In affected muscles, needle-electrode examination reveals widespread broad and polyphasic motor unit potentials (MUPs) firing in a reduced or rapid neurogenic recruitment pattern. Superimposed low-amplitude, short-duration, and polyphasic MUPs may be present. These configuration changes may resemble myopathic MUPs, but in the case of spinal muscular atrophy are instead due to early MUP reinnervation. Fibrillation potentials may be seen in limb and paraspinal muscles and are most striking in early or progressive spinal muscular atrophy. In late-juvenile and adult-onset forms, active motor axon loss is sparse. Fasciculation potentials are uncommon, but spontaneously firing motor unit action potentials (MUAPs) at 5-15 Hz have been described as a unique feature of SMA I and II.

Mild pseudomyotonic discharges have been observed in patients older than 6 years. However, these discharges are not specific for etiology and may be seen in chronic neurogenic disorders.


Muscle biopsy may necessary to differentiate spinal muscular atrophies from other neuromuscular disorders if genetic analysis is unrevealing. Muscle selection should be centered on clinically affected muscles but not to such a degree that degeneration renders the tissue unrecognizable.

Adequate results can be obtained with open or needle biopsy as long as the physician has adequate experience in the procedure and in processing of the tissue.

Electron microscopy can be used to evaluate for storage diseases.

Histologic Findings

Histologic findings depend on the stage and progression of disease. Initial changes include atrophy of muscle fibers with compensatory hypertrophy. This results in groups of large and small fibers (fiber-type grouping).

During the first 6-8 weeks of life, differentiating congenital fiber type disproportion and SMA may be difficult. In the chronic forms of SMA, secondary myopathic changes may be seen in addition to type grouping and may histologically resemble the muscular dystrophies.[43, 44]

Classic histologic findings include the following:

Medical Care

In December 2016, the FDA approved nusinersen (Spinraza), the first drug approved to treat children (including newborns) and adults with SMA. Nusinersen is an antisense oligonucleotide (ASO) designed to treat SMA caused by mutations in chromosome 5q that lead to SMN protein deficiency. Using in vitro assays and studies in transgenic animal models of SMA, nusinersen was shown to increase exon 7 inclusion in SMN2 messenger ribonucleic acid (mRNA) transcripts and production of full-length SMN protein.[45]

Nusinersen approval was based on the ENDEAR trial. The ENDEAR trial (n=121) is a phase 3 randomized, double-blind, sham-controlled study in patients with infantile-onset (most likely to develop Type 1) SMA. At a planned interim analysis, a greater percentage of infants treated with nusinersen achieved a motor milestone response compared to those who did not receive treatment (40% vs 0%; p< 0.0001) as measured by the Hammersmith Infant Neurological Examination (HINE). Additionally, a smaller percentage of patients in the nusinersen group died (23%) compared to untreated patients (43%).[46]

Interim data from another phase 3 trial, CHERISH, included 126 nonambulatory patients with later-onset SMA (consistent with Type 2), including patients with the onset of signs and symptoms at >6 months and an age of 2 to 12 years at screening. Prespecified interim analysis demonstrated a difference of 5.9 points (p= 0.0000002) at 15 months between the treatment (n=84) and sham-controlled (n=42) study arms, as measured by the Hammersmith Functional Motor Scale Expanded (HFMSE). From baseline to 15 months of treatment, patients in the nusinersen group achieved a mean improvement of 4.0 points in the HFMSE, while patients who were not on treatment declined by a mean of 1.9 points.[47]

Onasemnogene abeparvovec (Zolgensma) is a recombinant AAV9-based gene therapy designed to deliver a copy of the gene encoding the human survival motor neuron (SMN) protein. It is indicated for gene replacement therapy in children aged 2 years or younger with spinal muscular atrophy (SMA) type 1 (also called Werdnig-Hoffman disease) who have biallelic mutation in the survival motor neuron 1 (SNM1) gene.

Approval was based on the ongoing phase 3 STR1VE trial and the completed phase 1 START trial. Fifteen patients with SMA1 received a single dose of intravenous adeno-associated virus serotype 9 carrying SMN complementary DNA encoding the missing SMN protein. As of the data cutoff, all 15 patients were alive and event-free at 20 months of age, as compared with a rate of survival of 8% in a historical cohort. In the high-dose cohort, a rapid increase from baseline in the score on the CHOP INTEND scale followed gene delivery, with an increase of 9.8 points at 1 month and 15.4 points at 3 months, as compared with a decline in this score in a historical cohort. Of the 12 patients who had received the high dose, 11 sat unassisted, 9 rolled over, 11 fed orally and could speak, and 2 walked independently. Elevated serum aminotransferase levels occurred in 4 patients and were attenuated by prednisolone.[48]

Interim data analysis from the ongoing phase 3 STR1VE trial described 21 of 22 (95%) patients were alive and event-free. The median age was 9.5 months, with 6 of 7 (86%) patients aged 0.5 months or older surviving event-free. Interim results also showed ongoing improvement of motor milestones (eg, holding head erect, rolling over, sitting without support).[49, 50]

Medications such as valproic acid, phenylbutyrate, hydroxyurea, and albuterol have been shown to increase SMN transcription in laboratory studies, but clinical trials have not demonstrated significant improvement in disease progression. The SMA CARNIVAL trials (parts 1 and 2)[51, 52] found valproic acid and L-carnitine ineffective with regard to strength or functional improvement at 6 months and 12 months in both ambulatory and nonambulatory children. Adverse effects were reported in 85% of patients.[51] Gabapentin, riluzole, and olesoxime have been studied for their suspected neuroprotective properties, without significant clinical benefit noted.[38, 53, 54] Treatment with creatine, phenylbutyrate, gabapentin, thyrotropin-releasing hormone, and hydroxyurea have also proved ineffective.[53]

A randomized, double-blind, placebo-controlled trial in male subjects with genetically confirmed spinobulbar muscular atrophy (Kennedy disease) using oral dutasteride (a 5-alpha-reductase inhibitor that reduces dihydrotestosterone) did not show a significant effect on the progression of muscle weakness.[55] Failure of this treatment trial in spinobulbar muscular atrophy may in part be attributed to the underpowered study and the relatively short period in which treatment effect can be accurately measured because of the slowly progressive nature of this disease. These results also suggest that the role of androgens in spinobulbar muscular atrophy is complex.

Supportive treatment should be aimed at improving the patients' quality of life and minimizing disability, particularly in patients with slow progression.

The goals are to maximize the patient's independence and quality of life at each stage of the disease.

The treatment of patients with adult-onset spinal muscular atrophy is similar to that for amyotrophic lateral sclerosis (ALS), except that the course and life span in spinal muscular atrophies is considerably longer.

A multidisciplinary approach is essential. Once diagnosis is reached, overnight oximetry, respiratory muscle function tests, cough effectiveness, forced vital capacity (for patients >5 years), swallow study with video, physical and occupational therapy assessments, assistive equipment evaluation, and hip/spine radiography are appropriate. Recognition of mandibular dysfunction manifested as limited mouth opening is an important factor in prevention of aspiration.[38, 56]

Interventions such as chest physiotherapy, assisted cough, nocturnal (+/- daytime) noninvasive ventilation, and Nissen fundoplication for nonsitting patients may be considered. Gastrostomy placement is often pursued at the time of diagnosis for SMA1.[38]

The use of splints, bracing, and spinal orthoses can be customized to each patient.[57] Wheelchair use should be determined by patient’s level of fatigue with activity as well as their rate of falling.[38]

Women with SMA who become pregnant have no increased risk of miscarriage or hypertensive diseases. Higher rates of caesarian delivery (42.5%) and preterm deliveries (29.4%) have been observed. Approximately one third of patients noted deterioration of symptoms during pregnancy.[13]

Patients and families can also be directed to ongoing clinical trials for the treatment of spinal muscular atrophies. Descriptions of various trials can be found at the following Web sites:

Surgical Care

Surgical revision may provide stable correction of the spine, and early orthopedic intervention may be indicated in patients in whom prolonged survival is anticipated. Hip subluxations and dislocations are common. Nonsurgical treatment is generally preferred unless pain is severe, owing to the high rate of repeated dislocation.[58]

Noninvasive ventilation and percutaneous gastrostomy reportedly improves the quality of life with no effect on survival. These modalities may be most effective in prolonging lifespan in patients with slowly progressive disease, whereas they may provide comfort care in rapidly progressive infantile forms.[59]


Consultations for ancillary evaluations and treatments are appropriate. Consult the following specialists as needed: physical therapist, occupational therapist, speech therapist, dietary or nutritional therapist, social service staff, pulmonologist, orthopedics, and gastroenterologist. Palliative care consultation may be considered upon diagnosis of SMA1.[38]


Ensuring optimal caloric intake enables patients to use weak muscles to their maximum capacity without incurring obesity as a comorbid condition.


Encourage mobility. The goal of active but nonfatiguing exercises is to maintain range of motion, increase muscle flexibility, and prevent contractures. These exercises should not produce pain or exhaustion. A small series showed that the risk of falls is strongly correlated to stride-length variability, so this variable should be a focus of physical therapy programs.[60]

Preventing spinal deformities (eg, scoliosis) and joint contractures is important. This goal is accomplished by using range-of-motion exercises, knee-ankle-foot orthoses, specialized wheelchairs and seats at home and school, and home assistance devices.

Medication Summary

In December 2016, the FDA approved nusinersen, the first drug approved to treat children (including newborns) and adults with spinal muscular atrophy (SMA). The recombinant AAV9-based gene therapy, onasemnogene abeparvovec, was approved in May 2019 for SMA type 1 in children aged 2 years or younger.

Nusinersen (Spinraza)

Clinical Context:  In studies in transgenic animal models of SMA, nusinersen was shown to increase exon 7 inclusion in SMN2 messenger ribonucleic acid (mRNA) transcripts and production of full-length SMN protein. It is indicated for SMA in pediatric and adults patients.

Class Summary

Antisense oligonucleotides (ASO) designed to treat SMA caused by mutations in chromosome 5q that lead to SMN protein deficiency may be considered for treatment.

Onasemnogene abeparvovec (Zolgensma)

Clinical Context:  Recombinant AAV9-based gene therapy designed to deliver a copy of the gene encoding the human survival motor neuron (SMN) protein. It is indicated for gene replacement therapy in children aged 2 years or younger with spinal muscular atrophy (SMA) type 1 (also called Werdnig-Hoffman disease) who have biallelic mutation in the survival motor neuron 1 (SMN1) gene.

Class Summary

Recombinant gene therapy provides specificity to precisely treat gene deficiency.


Genetic counseling should be offered to all families of patients with spinal muscular atrophy. Obtaining a complete family history facilitates genetic counseling. Carrier testing is available for commercial use. A recent study of 68,471 individuals showed that carrier-status testing may be feasible given the high carrier prevalence (1 in 54 overall).[61]

Education on how the disease is inherited may avert conception of affected individuals.

Furthermore, the role of prenatal diagnosis, particularly in pregnant carriers or those with juvenile or adult-onset forms, should also be addressed.


Medical complications associated with the SMAs include pulmonary infections, spinal deformities (eg, scoliosis, hip subluxations/dislocations), joint contractures, and respiratory failure.


See Mortality/Morbidity for more information.

Most patients with SMA type I die before 18 months of age. In contrast, outcomes of juvenile and adult spinal muscular atrophies are difficult to define because the progression of these diseases varies widely.

Survival probabilities for types I and II and probabilities of being ambulatory for type III were derived for 445 patients. These patients were subdivided on the basis of ISMAC criteria (ie, developmental milestones and age of onset).[62]

A recent series of 237 patients showed similar survival probabilities.[63]

Disease onset after age 2-3 months has been correlated to longer survival time in SMA type I.[64, 63] Antibiotic treatment has not prolonged survival in SMA type I. Birnkrant et al examined the role of noninvasive positive-pressure ventilation and gastrostomy in patients with SMA type I. Although these supportive measures can be effective in slowly progressive neuromuscular diseases, they did not alter survival in patients with SMA type I.[59] A later study by Lemoine et al concluded that early noninvasive respiratory intervention prolonged survival time compared with supportive care alone.[65]

Patient Education

Normal schooling in patients with SMA, especially types II and II or more indolent forms, is highly recommended because their intelligence is normal or even superior to that of other individuals.

Support groups are available in some locations for patients and their families.

What is spinal muscular atrophy (SMA)?What is the pathophysiology of spinal muscular atrophy (SMA)?What is the prevalence of spinal muscular atrophy (SMA) in the US?What is the global prevalence of spinal muscular atrophy (SMA)?What is the mortality and morbidity associated with spinal muscular atrophy (SMA)?What are the sexual predilections of spinal muscular atrophy (SMA)?What is the age of onset of spinal muscular atrophy (SMA)?Which clinical history findings are characteristic of spinal muscular atrophy (SMA)?Which clinical history findings are characteristic of spinal muscular atrophy (SMA) type I - acute infantile or Werdnig-Hoffman disease?Which clinical history findings are characteristic of spinal muscular atrophy (SMA) type II - chronic infantile form?Which clinical history findings are characteristic of spinal muscular atrophy (SMA) type III - chronic juvenile or Kugelberg-Welander syndrome?Which clinical history findings are characteristic of spinal muscular atrophy (SMA) type IV - adult-onset form?Which physical findings are characteristic of spinal muscular atrophy (SMA)?Which physical findings are characteristic of spinal muscular atrophy (SMA) type I - acute infantile or Werdnig-Hoffman disease?Which physical findings are characteristic of spinal muscular atrophy (SMA) type II - chronic infantile form?Which physical findings are characteristic of spinal muscular atrophy (SMA) type III - chronic juvenile or Kugelberg-Welander syndrome?Which physical findings are characteristic of spinal muscular atrophy (SMA) type IV - adult-onset form?What are the variants of spinal muscular atrophy (SMA)?What causes spinal muscular atrophy (SMA)?What are the differential diagnoses for Spinal Muscular Atrophy?Which lab test results are characteristic of spinal muscular atrophy (SMA)?What is the role of genetic testing in the workup of spinal muscular atrophy (SMA)?Which findings on ECG are characteristic of spinal muscular atrophy (SMA)?What is the role of NCS in the workup of spinal muscular atrophy (SMA)?What is the role of EMG in the workup of spinal muscular atrophy (SMA)?What is the role of biopsy in the workup of spinal muscular atrophy (SMA)?Which histologic findings are characteristic of spinal muscular atrophy (SMA)?How is spinal muscular atrophy (SMA) treated?Where is information about spinal muscular atrophy (SMA) clinical trials found?What is the role of surgery in the treatment of spinal muscular atrophy (SMA)?Which specialist consultations are beneficial to patients with spinal muscular atrophy (SMA)?Which dietary modifications are used in the treatment of spinal muscular atrophy (SMA)?Which activity modifications are used in the treatment of spinal muscular atrophy (SMA)?What is the role of nusinersen in the treatment of spinal muscular atrophy (SMA)?Which medications in the drug class Antisense Oligonucleotides are used in the treatment of Spinal Muscular Atrophy?Which medications in the drug class Gene Therapy are used in the treatment of Spinal Muscular Atrophy?How is spinal muscular atrophy (SMA) prevented?What are the possible complications of spinal muscular atrophy (SMA)?What is the prognosis of spinal muscular atrophy (SMA)?What is included in patient education about spinal muscular atrophy (SMA)?


Jeffrey Rosenfeld, MD, PhD, FAAN, Professor of Neurology, Associate Chairman, Department of Neurology, Director, Neuromuscular ALS/MND Program, Medical Director, The Center for Restorative Neurology, Loma Linda University Health Systems

Disclosure: Nothing to disclose.


Carmel Armon, MD, MSc, MHS, Chair, Department of Neurology, Assaf Harofeh Medical Center, Tel Aviv University Sackler Faculty of Medicine, Israel

Disclosure: Received research grant from: Neuronix Ltd, Yoqnea'm, Israel<br/>Received income in an amount equal to or greater than $250 from: JNS - Associate Editor. UpToDate - Author Royalties.

Specialty Editors

Francisco Talavera, PharmD, PhD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Chief Editor

Stephen L Nelson, Jr, MD, PhD, FAACPDM, FAAN, FAAP, Chief, Pediatric Neurology, Professor of Pediatrics, Neurology, Neurosurgery, and Psychiatry, Epileptologist, Medical Director, Tulane Center for Autism and Related Disorders, Co-Director, Developmental Neurogenetics Center, Tulane University School of Medicine

Disclosure: Serve(d) as a speaker or a member of a speakers bureau for: Biomarin; Supernus<br/>Received income in an amount equal to or greater than $250 from: Biomarin; Supernus; American Board of Pediatrics.

Additional Contributors

Bryan Tsao, MD, Associate Professor, Department of Neurology, Loma Linda University; Chair and Service Chief, Department of Neurology, Loma Linda University Medical Center

Disclosure: Nothing to disclose.

Robert J Baumann, MD, Professor of Neurology and Pediatrics, Department of Neurology, University of Kentucky College of Medicine

Disclosure: Nothing to disclose.

Theresa L LaBarte, DO, Resident Physician, Department of Neurology, Loma Linda University Medical Center

Disclosure: Nothing to disclose.


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