Medicine:Spinal muscular atrophies

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Short description: Group of disorders
Spinal muscular atrophies
Polio spinal diagram-en.svg
Location of neurons affected in spinal muscular atrophies
SpecialtyNeurology
SymptomsLoss of motor neurons resulting in muscle wasting

Spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of rare debilitating disorders characterised by the degeneration of lower motor neurons (neuronal cells situated in the anterior horn of the spinal cord) and subsequent atrophy (wasting) of various muscle groups in the body.[1] While some SMAs lead to early infant death, other diseases of this group permit normal adult life with only mild weakness.

Classification

Based on the type of muscles affected, spinal muscular atrophies can be divided into:[citation needed]

When taking into account prevalence, spinal muscular atrophies are traditionally divided into:[citation needed]

  • Autosomal recessive proximal spinal muscular atrophy, responsible for 90-95% of cases and usually called simply spinal muscular atrophy (SMA) – a disorder associated with a genetic mutation on the SMN1 gene on chromosome 5q (locus 5q13), diagnosed predominantly in young children and in its most severe form being the most common genetic cause of infant death if left untreated;
  • Localised spinal muscular atrophies – much more rare conditions, in some instances described in but a few patients in the world, which are associated with mutations of genes other than SMN1 and for this reason sometimes termed simply non-5q spinal muscular atrophies; none has currently a causal treatment.

A more detailed classification is based on the gene associated with the condition (where identified) and is presented in table below.

Group Name
Alternative names
OMIM Gene Locus Mode of
inheritance
Characteristics
SMA Spinal muscular atrophy (SMA)
  • 5q spinal muscular atrophy
  • Autosomal recessive proximal spinal muscular atrophy
  • Werdnig–Hoffmann disease / Kugelberg–Welander disease
Online Mendelian Inheritance in Man (OMIM) 253300
Online Mendelian Inheritance in Man (OMIM) 253550
Online Mendelian Inheritance in Man (OMIM) 253400
Online Mendelian Inheritance in Man (OMIM) 271150
SMN1 5q13.2 Autosomal recessive Affects primarily proximal muscles in people of all ages, progressive, relatively common
XLSMA X-linked spinal muscular atrophy type 1 (SMAX1)
  • Spinal and bulbar muscular atrophy (SBMA)
  • Kennedy's disease (KD)
Online Mendelian Inheritance in Man (OMIM) 313200 NR3C4 Xq12 X-linked recessive Affects primarily bulbar muscles as well as sensory nerves mainly in adult men, progressive
X-linked spinal muscular atrophy type 2 (SMAX2)
  • Arthrogryposis multiplex congenita – X-linked type 1 (AMCX1)
Online Mendelian Inheritance in Man (OMIM) 301830 UBA1 Xp11.23 X-linked recessive Characterised by bone fractures, affects mainly distal muscles in newborn boys, usually fatal in infancy
X-linked spinal muscular atrophy type 3 (SMAX3)
  • Distal spinal muscular atrophy – X-linked (DSMAX)
Online Mendelian Inheritance in Man (OMIM) 300489 ATP7A Xq21.1 X-linked recessive Affects distal muscles of all extremities mainly in boys, slowly progressive
DSMA Distal spinal muscular atrophy type 1 (DSMA1)
  • Spinal muscular atrophy with respiratory distress type 1 (SMARD1)
  • Distal hereditary motor neuronopathy type 6 (DHMN6)
Online Mendelian Inheritance in Man (OMIM) 604320 IGHMBP2 11q13.3 Autosomal recessive Affects mainly infant boys, similar to SMA type 1 but with diaphragmatic paralysis
Distal spinal muscular atrophy type 2 (DSMA2)
  • Distal hereditary motor neuronopathy – Jerash type (DHMN-J)
Online Mendelian Inheritance in Man (OMIM) 605726 SIGMAR1 19p13.3 Autosomal recessive Slowly progressive
Distal spinal muscular atrophy type 3 (DSMA3)
  • Distal hereditary motor neuronopathy types 3 & 4 (DHMN3/DHMN4)
Online Mendelian Inheritance in Man (OMIM) 607088 ? 11q13.3 Autosomal recessive Slowly progressive
Distal spinal muscular atrophy type 4 (DSMA4) Online Mendelian Inheritance in Man (OMIM) 611067 PLEKHG5 1p36.31 Autosomal recessive Slowly progressive, described only in one family
Distal spinal muscular atrophy type 5 (DSMA5) Online Mendelian Inheritance in Man (OMIM) 614881 DNAJB2 2q35 Autosomal recessive Young adult onset, slowly progressive
Distal spinal muscular atrophy type VA (DSMAVA)
  • Distal hereditary motor neuronopathy type 5A (DHMN5A)
Online Mendelian Inheritance in Man (OMIM) 600794 GARS 7p14.3 Autosomal dominant With upper limb predominance; allelic and overlapping with CMT2D, phenotype overlapping with Silver syndrome
Distal spinal muscular atrophy type VB (DSMAVB)
  • Distal hereditary motor neuronopathy type 5B (DHMN5B)
Online Mendelian Inheritance in Man (OMIM) 614751 REEP1 2p11 Autosomal dominant With upper limb predominance; allelic and overlapping with HSP-31
Distal spinal muscular atrophy with calf predominance
  • Distal hereditary motor neuronopathy type 2D (DHMN2D)
Online Mendelian Inheritance in Man (OMIM) 615575 FBXO38 5q32 Autosomal dominant Juvenile- or adult-onset, slowly progressive, affects both proximal and distal muscles, initially manifests with calf weakness which progresses to hands
Distal spinal muscular atrophy with vocal cord paralysis
  • Distal hereditary motor neuronopathy type 7A (DHMN7A)
  • Harper–Young myopathy
Online Mendelian Inheritance in Man (OMIM) 158580 SLC5A7 2q12.3 Autosomal dominant Adult-onset with vocal cord paralysis, very rare
Congenital distal spinal muscular atrophy
  • Distal hereditary motor neuronopathy type 8 (DHMN8)
Online Mendelian Inheritance in Man (OMIM) 600175 TRPV4 12q24.11 Autosomal dominant Affects primarily distal muscles of lower limbs, non-progressive, rare, allelic with SPSMA and CMT2C
Scapuloperoneal spinal muscular atrophy (SPSMA)
  • Scapuloperoneal neurogenic amyotrophy
Online Mendelian Inheritance in Man (OMIM) 181405 TRPV4 12q24.11 Autosomal dominant
or X-linked dominant
Affects muscles of lower limbs, non-progressive, rare, allelic with congenital distal spinal muscular atrophy and CMT2C
Autosomal dominant distal spinal muscular atrophy
  • Distal hereditary motor neuronopathy type 2A (DHMN2A)
Online Mendelian Inheritance in Man (OMIM) 158590 HSPB8 12q24.23 Autosomal dominant Adult-onset. Allelic with Charcot–Marie–Tooth disease type 2L (CMT2L)
Autosomal dominant juvenile distal spinal muscular atrophy
  • Distal hereditary motor neuronopathy type 1 (DHMN1)
Online Mendelian Inheritance in Man (OMIM) 182960 ? 7q34–q36 Autosomal dominant Juvenile-onset
Juvenile segmental spinal muscular atrophy (JSSMA) Online Mendelian Inheritance in Man (OMIM) 183020 ? 18q21.3 ? Juvenile-onset, progressive with stabilisation after 2–4 years, affects primarily hands, very rare
Finkel type proximal spinal muscular atrophy (SMAFK) Online Mendelian Inheritance in Man (OMIM) 182980 VAPB 20q13.32 Autosomal dominant Late-onset, affects proximal muscles in adults
James type infantile spinal muscular atrophy (SMAJI) Online Mendelian Inheritance in Man (OMIM) 619042 GARS1 7p14.3 Autosomal dominant Infantile-onset hypotonia, slowly progressive, resulting in delayed motor milestones and loss of previous motor skills. Children never walk. Milder disorders caused by GARS1 mutations are CMT2D and HMN5A.
Jokela type spinal muscular atrophy (SMAJ) Online Mendelian Inheritance in Man (OMIM) 615048 CHCHD10 22q11.2–q13.2 Autosomal dominant Late-onset, slowly progressive, affects both proximal and distal muscles in adults
Spinal muscular atrophy with lower extremity predominance 1 (SMALED1) Online Mendelian Inheritance in Man (OMIM) 158600 DYNC1H1 14q32 Autosomal dominant Affects proximal muscles in infants
Spinal muscular atrophy with lower extremity predominance 2A (SMALED2A) Online Mendelian Inheritance in Man (OMIM) 615290 BICD2 9q22.31 Autosomal dominant Early-onset, primarily affecting lower limbs, slowly progressive, non-life-limiting, very rare
Spinal muscular atrophy with lower extremity predominance 2B (SMALED2B) Online Mendelian Inheritance in Man (OMIM) 618291 BICD2 9q22.31 Autosomal dominant Presents with hypotonia, contractures and respiratory involvement at birth, frequently fatal in early childhood, very rare
Spinal muscular atrophy with progressive myoclonic epilepsy (SMAPME) Online Mendelian Inheritance in Man (OMIM) 159950 ASAH1 8p22 Autosomal recessive
Spinal muscular atrophy with congenital bone fractures 1 (SMABF1) Online Mendelian Inheritance in Man (OMIM) 616866 TRIP4 15q22.31 Autosomal recessive Prenatal onset, characterised by severe muscle wasting, respiratory and feeding failure, and bone fractures at birth as in arthrogryposis multiplex congenita, usually fatal in infancy
Spinal muscular atrophy with congenital bone fractures 2 (SMABF2) Online Mendelian Inheritance in Man (OMIM) 616867 ASCC1 10q22.1 Autosomal recessive Prenatal onset, characterised by severe muscle wasting, respiratory and feeding failure, and bone fractures at birth as in arthrogryposis multiplex congenita, usually fatal in infancy[2][3][4]
PCH Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH)
  • Pontocerebellar hypoplasia type 1A (PCH1A)
Online Mendelian Inheritance in Man (OMIM) 607596 VRK1 14q32 Autosomal dominant → see Pontocerebellar hypoplasia
MMA Juvenile asymmetric segmental spinal muscular atrophy (JASSMA)
  • Monomelic amyotrophy
  • Hirayama disease
  • Sobue disease
Online Mendelian Inheritance in Man (OMIM) 602440 ? ? ? → see Monomelic amyotrophy
PMA Progressive spinal muscular atrophy
  • Progressive muscular atrophy
  • Duchenne-Aran muscular atrophy
? ? ? ? → see Progressive muscular atrophy

In all forms of SMA (with an exception of X-linked spinal muscular atrophy type 1), only motor neurons, located at the anterior horn of spinal cord, are affected; sensory neurons, which are located at the posterior horn of spinal cord, are not affected. By contrast, hereditary disorders that cause both weakness due to motor denervation along with sensory impairment due to sensory denervation are known as hereditary motor and sensory neuropathies (HMSN).[citation needed]

See also

References

  1. "Spinal muscular atrophy". 2016-03-21. https://ghr.nlm.nih.gov/condition/spinal-muscular-atrophy. 
  2. "Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures". American Journal of Human Genetics 98 (3): 473–489. March 2016. doi:10.1016/j.ajhg.2016.01.006. PMID 26924529. 
  3. "The new neuromuscular disease related with defects in the ASC-1 complex: report of a second case confirms ASCC1 involvement". Clinical Genetics 92 (4): 434–439. October 2017. doi:10.1111/cge.12997. PMID 28218388. 
  4. "A new case of SMABF2 diagnosed in stillbirth expands the prenatal presentation and mutational spectrum of ASCC1". American Journal of Medical Genetics. Part A 182 (3): 508–512. December 2019. doi:10.1002/ajmg.a.61431. PMID 31880396. 

Further reading

External links

Classification