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Vidovic, M.; Müschen, L.H.; Brakemeier, S.; Machetanz, G.; Naumann, M.; Castro-Gomez, S. Clinical Presentation of Amyotrophic Lateral Sclerosis. Encyclopedia. Available online: https://encyclopedia.pub/entry/41858 (accessed on 03 December 2024).
Vidovic M, Müschen LH, Brakemeier S, Machetanz G, Naumann M, Castro-Gomez S. Clinical Presentation of Amyotrophic Lateral Sclerosis. Encyclopedia. Available at: https://encyclopedia.pub/entry/41858. Accessed December 03, 2024.
Vidovic, Maximilian, Lars Hendrik Müschen, Svenja Brakemeier, Gerrit Machetanz, Marcel Naumann, Sergio Castro-Gomez. "Clinical Presentation of Amyotrophic Lateral Sclerosis" Encyclopedia, https://encyclopedia.pub/entry/41858 (accessed December 03, 2024).
Vidovic, M., Müschen, L.H., Brakemeier, S., Machetanz, G., Naumann, M., & Castro-Gomez, S. (2023, March 03). Clinical Presentation of Amyotrophic Lateral Sclerosis. In Encyclopedia. https://encyclopedia.pub/entry/41858
Vidovic, Maximilian, et al. "Clinical Presentation of Amyotrophic Lateral Sclerosis." Encyclopedia. Web. 03 March, 2023.
Clinical Presentation of Amyotrophic Lateral Sclerosis
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This entry is adapted from the peer-reviewed paper 10.3390/cells12050736

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by loss of upper and lower motor neurons, resulting in progressive weakness of all voluntary muscles and eventual respiratory failure. Non-motor symptoms, such as cognitive and behavioral changes, frequently occur over the course of the disease.

amyotrophic lateral sclerosis ALS motor neuron disease MND diagnosis clinical presentation diagnostics symptoms

1. Introduction

The diagnosis of amyotrophic lateral sclerosis (ALS) remains an enormous challenge not only to general physicians, but also to specialized neurologists. ALS, a fatal neurodegenerative and the most frequent motor neuron disease (MND), is primarily characterized by progressive weakness of voluntary muscles due to degenerating motor neurons in the brain, brainstem and spinal cord. Considered to be a multisystem disorder, it can also be accompanied by non-motor symptoms, such as behavioral and cognitive impairment, and even manifest as an overlap syndrome with signs of frontotemporal dementia (FTD), known as ALS-FTD [1][2][3].

2. Clinical Presentation

It is essential to record the clinical findings and their course as accurately as possible. Therefore, a thorough exploration of the patient’s history of symptoms and a complete physical and neurological examination should be considered as the first step in the diagnosis of ALS.
The clinical hallmarks of ALS are related to the impairment of voluntary muscles, resulting in progressive weakness of the limbs, speech and swallowing dysfunction and respiratory failure with concomitant signs, such as muscle atrophy, fasciculations and increased muscle tone. These motor dysfunctions are derived from the combined impairment of the upper motor neurons (UMN) in the motor cortex of the brain and the lower motor neurons (LMN) in the brainstem and the spinal cord [1][3]. Though generally unaffected, there is also evidence of oculomotor, sphincter and autonomic dysfunction [4][5]. Initially, the disease typically presents itself either with asymmetrical focal muscle weakness in the upper or lower limbs in spinal onset ALS or with speech and swallowing difficulties due to facial, tongue and pharyngeal muscle weakness in bulbar-onset ALS [2]. Disease propagation preferably follows an organized contiguous pattern with first symptoms in one limb, subsequently spreading to the contralateral limb and, later, to adjacent regions [6]. However, disease progression is highly variable and frequently shows a non-linear decline [7]. The anatomically separated body regions (or segments) are defined as the bulbar, cervical, thoracic and lumbar regions, with the latter three comprising the spinal regions [8].
The clinical signs of UMN and LMN involvement according to each of the body regions are presented in Figure 1.
Figure 1. Clinical signs of UMN and LMN involvement according to body regions. DTR: Deep tendon reflex; LMN: Lower motor neurons; UMN: Upper motor neurons. Created by Castro-Gomez with “BioRender.com”; accessed on 4 February 2023.
The notable clinical heterogeneity of motor manifestations frequently leads to controversy in the description of phenotypes as opposed to the determination of the diagnosis of ALS. Distinguishing these phenotypes is of relevance, as they are associated with various disease progression rates and survival times [9].
The different clinical phenotypes of ALS are generally described with regard to the extent of UMN and LMN impairment, its distribution and progression to the different body segments [2][9].

2.1. Spinal-Onset ALS

ALS with spinal onset is defined by focal weakness in distal muscle groups of the limbs and simultaneous UMN and LMN involvement. With up to 82% of all ALS patients [10], it is the most common phenotype, termed typical or classical ALS. Distal segments of the upper or lower limbs are affected in a focal manner at the onset of the disease. Characteristically, thenar eminence with the abductor pollicis brevis (APB) and the first dorsal interosseus (FDI) muscles are more affected compared to the hypothenar muscle abductor digiti minimi (ADM), referred to as split-hand syndrome [11]. Onset in the dominant hand is thought to be predominant [12]. Lower-limb weakness typically becomes apparent as it causes an unsteady gait due to weak foot dorsiflexion [13]. Notably, UMN dysfunction is not always easily identified in wasted or atrophic muscles of the limbs, particularly in the early stages of the disease [14][15].

2.2. Bulbar-Onset ALS

ALS with bulbar onset, or bulbar ALS, is the second leading phenotype with initial motor dysfunction in the bulbar region. Speech difficulties and frequent choking with concomitant hypersalivation are the cardinal presenting symptoms. Both LMN and UMN impairment are present, causing tongue wasting with fasciculations, facial spasticity and pseudobulbar affect in the early stages of the disease. Propagation to other spinal regions is evident later in the disease’s course [16]. Bulbar UMN involvement, also known as pseudobulbar palsy, can become clinically indicated by emotional lability, accompanied by excessive crying or laughing response to minor stimuli. This is termed the “pseudobulbar affect”. Other bulbar UMN signs include facial spasticity and slowed spastic movement of the tongue, whereas slurred speech, wasting of the tongue and fasciculations indicate bulbar LMN impairment [1][3]. Frontal release signs, such as the palmomental reflex, may also indicate bulbar involvement [17]. In contrast to the often used phrase “progressive bulbar palsy”, “ALS with bulbar onset” appears to be the more convenient term, as it represents a phenotypic description rather than a diagnostic label, suggesting no progression to other body regions [9].

2.3. Progressive Muscular Atrophy

Progressive muscular atrophy (PMA) presents with clinically isolated LMN impairment of the anterior horn cells and brainstem motor nuclei. However, subclinical UMN impairment can be detected in the early stages of the disease [18]. Although PMA tends to have a slower disease progression than classical ALS [19], 20 to 30% of the patients may develop ALS with clinically evident UMN impairment within 5 to 10 years from the disease’s onset. It is still controversially debated whether PMA should be considered a variant of ALS [18].

2.4. Primary Lateral Sclerosis

Primary lateral sclerosis (PLS) is characterized by progressive isolated UMN dysfunction detectable in at least two regions (thoracic region will not be considered) for at least two years. LMN dysfunction is absent, whereas minimal signs of denervation (positive sharp waves or fibrillation potentials) on electromyography (EMG) are permitted. Whether PLS constitutes a separate disease entity or rather represents a clinically benign variant of ALS remains controversial [20].

2.5. Flail-Arm-Syndrome

In flail-arm-syndrome (FAS), also known as Vulpian Bernhardt’s type, progressive, proximal and symmetrical weakness of both upper limbs caused by LMN impairment is predominantly apparent. Motor symptoms in bulbar muscles or lower limbs are unaffected from 12 to 20 months after the onset of upper limb symptoms [21][22]. LMN involvement is predominant, whereas UMN involvement can be occasionally present in lower limbs [23]. FAS represents a rather benign phenotype with a median survival time of 4 years and a 10 year survival rate of 17% [21].

2.6. Flail-Leg-Syndrome

Analogous to FAS, flail-leg-syndrome (FLS) presents itself with progressive and symmetrical weakness of both lower limbs, whereas distal muscle groups are typically affected and LMN involvement outweighs UMN involvement [22]. Other segments are clinically spared for a mean of 16 months after the disease’s onset. Unlike FAS, FLS has a similar prognosis as spinal-onset ALS, with a median survival time of 3 years and a 10-year survival rate of 13% [21].

2.7. Axial or Respiratory-Onset ALS

Axial-onset ALS initially presents itself with weakness of trunk muscles. Typically, paravertebral muscles are affected, resulting in bent posture, axial instability and dropped head syndrome [24]. However, weakness of the thoracic muscles can be rather difficult to recognize [6].
In respiratory-onset ALS patients suffer from dyspnoea and orthopnoea at the beginning of the disease, caused by weakness of the respiratory muscles and the diaphragm, which is also anatomically related to the thoracic region [25]. The prognosis is poor due to early respiratory failure and complications such as pneumonia [21][24][26].
There is no reliable method to detect thoracic UMN involvement [27]. However, brisk and deep abdominal reflexes, particularly with diminished or absent superficial abdominal reflexes, might be suggestive signs [28].

2.8. Hemiplegic ALS (Mill’s Syndrome)

This very rare phenotype is defined by slowly progressive, unilateral muscle weakness in the limbs alongside clinically predominant UMN signs, such as pathological deep tendon reflexes (DTR) and pyramidal tract signs. The onset may either occur in the upper limbs with subsequent descending propagation to the lower limbs or vice versa [29]. As is the case with PLS, there is an ongoing debate regarding whether Mill’s syndrome should be considered a distinct clinical entity in the spectrum of motor neuron diseases or an ALS variant [29][30][31].

References

  1. Brown, R.H.; Al-Chalabi, A. Amyotrophic Lateral Sclerosis. N. Engl. J. Med. 2017, 377, 162–172.
  2. Goutman, S.A.; Hardiman, O.; Al-Chalabi, A.; Chió, A.; Savelieff, M.G.; Kiernan, M.C.; Feldman, E.L. Recent Advances in the Diagnosis and Prognosis of Amyotrophic Lateral Sclerosis. Lancet Neurol. 2022, 21, 480–493.
  3. Feldman, E.L.; Goutman, S.A.; Petri, S.; Mazzini, L.; Savelieff, M.G.; Shaw, P.J.; Sobue, G. Amyotrophic Lateral Sclerosis. Lancet 2022, 400, 1363–1380.
  4. Weise, D.; Menze, I.; Metelmann, M.C.F.; Woost, T.B.; Classen, J.; Otto Pelz, J. Multimodal Assessment of Autonomic Dysfunction in Amyotrophic Lateral Sclerosis. Eur. J. Neurol. 2022, 29, 715–723.
  5. Sharma, R.; Hicks, S.; Berna, C.M.; Kennard, C.; Talbot, K.; Turner, M.R. Oculomotor Dysfunction in Amyotrophic Lateral Sclerosis: A Comprehensive Review. Arch. Neurol. 2011, 68, 857–861.
  6. Walhout, R.; Verstraete, E.; van den Heuvel, M.P.; Veldink, J.H.; van den Berg, L.H. Patterns of Symptom Development in Patients with Motor Neuron Disease. Amyotroph. Lateral Scler. Front. Degener. 2018, 19, 21–28.
  7. Ramamoorthy, D.; Severson, K.; Ghosh, S.; Sachs, K.; Glass, J.D.; Fournier, C.N.; Herrington, T.M.; Berry, J.D.; Ng, K.; Fraenkel, E. Identifying Patterns in Amyotrophic Lateral Sclerosis Progression from Sparse Longitudinal Data. Nat. Comput. Sci. 2022, 2, 605–616.
  8. Brooks, B.R. El Escorial World Federation of Neurology Criteria for the Diagnosis of Amyotrophic Lateral Sclerosis. J. Neurol. Sci. 1994, 124, 96–107.
  9. Al-Chalabi, A.; Hardiman, O.; Kiernan, M.C.; Chiò, A.; Rix-Brooks, B.; van den Berg, L.H. Amyotrophic Lateral Sclerosis: Moving towards a New Classification System. Lancet Neurol. 2016, 15, 1182–1194.
  10. Longinetti, E.; Fang, F. Epidemiology of Amyotrophic Lateral Sclerosis: An Update of Recent Literature. Curr. Opin. Neurol. 2019, 32, 771–776.
  11. Wilbourn, A.J. The “Split Hand Syndrome”. Muscle Nerve 2000, 23, 138.
  12. Turner, M.R.; Wicks, P.; Brownstein, C.A.; Massagli, M.P.; Toronjo, M.; Talbot, K.; Al-Chalabi, A. Concordance between Site of Onset and Limb Dominance in Amyotrophic Lateral Sclerosis. J. Neurol. Neurosurg. Psychiatry 2011, 82, 853–854.
  13. Hu, F.; Jin, J.; Chen, Q.; Kang, L.; Jia, R.; Qin, X.; Liu, X.; Dang, Y.; Dang, J. Dissociated Lower Limb Muscle Involvement in Amyotrophic Lateral Sclerosis and Its Differential Diagnosis Value. Sci. Rep. 2019, 9, 17786.
  14. Swash, M. Why Are Upper Motor Neuron Signs Difficult to Elicit in Amyotrophic Lateral Sclerosis? J. Neurol. Neurosurg. Psychiatry 2012, 83, 659–662.
  15. Huynh, W.; Simon, N.G.; Grosskreutz, J.; Turner, M.R.; Vucic, S.; Kiernan, M.C. Assessment of the Upper Motor Neuron in Amyotrophic Lateral Sclerosis. Clin. Neurophysiol. 2016, 127, 2643–2660.
  16. van Es, M.A.; Hardiman, O.; Chio, A.; Al-Chalabi, A.; Pasterkamp, R.J.; Veldink, J.H.; van den Berg, L.H. Amyotrophic Lateral Sclerosis. Lancet 2017, 390, 2084–2098.
  17. Vidovic, M.; Aust, E.; Hermann, A.; Günther, R. The Palmomental Reflex in Amyotrophic Lateral Sclerosis—A Clinical Sign of Executive or Motor Dysfunction? Amyotroph. Lateral Scler. Front. Degener. 2021, 22, 588–591.
  18. Liewluck, T.; Saperstein, D.S. Progressive Muscular Atrophy. Neurol. Clin. 2015, 33, 761–773.
  19. Kim, W.-K.; Liu, X.; Sandner, J.; Pasmantier, M.; Andrews, J.; Rowland, L.P.; Mitsumoto, H. Study of 962 Patients Indicates Progressive Muscular Atrophy Is a Form of ALS. Neurology 2009, 73, 1686–1692.
  20. Turner, M.R.; Barohn, R.J.; Corcia, P.; Fink, J.K.; Harms, M.B.; Kiernan, M.C.; Ravits, J.; Silani, V.; Simmons, Z.; Statland, J.; et al. Primary Lateral Sclerosis: Consensus Diagnostic Criteria. J. Neurol. Neurosurg. Psychiatry 2020, 91, 373–377.
  21. Chiò, A.; Calvo, A.; Moglia, C.; Mazzini, L.; Mora, G.; PARALS study group. Phenotypic Heterogeneity of Amyotrophic Lateral Sclerosis: A Population Based Study. J. Neurol. Neurosurg. Psychiatry 2011, 82, 740–746.
  22. Wijesekera, L.C.; Mathers, S.; Talman, P.; Galtrey, C.; Parkinson, M.H.; Ganesalingam, J.; Willey, E.; Ampong, M.A.; Ellis, C.M.; Shaw, C.E.; et al. Natural History and Clinical Features of the Flail Arm and Flail Leg ALS Variants. Neurology 2009, 72, 1087–1094.
  23. Hu, M.T.; Ellis, C.M.; Al-Chalabi, A.; Leigh, P.N.; Shaw, C.E. Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis. J. Neurol. Neurosurg. Psychiatry 1998, 65, 950–951.
  24. Masrori, P.; Van Damme, P. Amyotrophic Lateral Sclerosis: A Clinical Review. Eur. J. Neurol. 2020, 27, 1918–1929.
  25. De Carvalho, M.; Pinto, S.; Swash, M. Association of Paraspinal and Diaphragm Denervation in ALS. Amyotroph. Lateral Scler. Off. Publ. World Fed. Neurol. Res. Group Mot. Neuron Dis. 2010, 11, 63–66.
  26. Swinnen, B.; Robberecht, W. The Phenotypic Variability of Amyotrophic Lateral Sclerosis. Nat. Rev. Neurol. 2014, 10, 661–670.
  27. Johnsen, B. Diagnostic Criteria for Amyotrophic Lateral Sclerosis from El Escorial to Gold Coast. Clin. Neurophysiol. Off. J. Int. Fed. Clin. Neurophysiol. 2020, 131, 1962–1963.
  28. Kee, R.; O’Gorman, C.M. Teaching Video NeuroImages: The Pathologic Deep Abdominal Reflex. Neurology 2017, 89, e245.
  29. Rajabally, Y.A.; Hbahbih, M.; Abbott, R.J. Hemiplegic ALS: Mills Syndrome. Neurology 2005, 64, 1984–1985.
  30. Jaiser, S.R.; Mitra, D.; Williams, T.L.; Baker, M.R. Mills’ Syndrome Revisited. J. Neurol. 2019, 266, 667–679.
  31. Gastaut, J.L.; Bartolomei, F. Mills’ Syndrome: Ascending (or Descending) Progressive Hemiplegia: A Hemiplegic Form of Primary Lateral Sclerosis? J. Neurol. Neurosurg. Psychiatry 1994, 57, 1280–1281.
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Subjects: Clinical Neurology
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Maximilian Vidovic
,
Lars Hendrik Müschen
,
Svenja Brakemeier
,
Gerrit Machetanz
,
Marcel Naumann
,
Sergio Castro-Gomez
View Times: 2.1K
Entry Collection: Neurodegeneration
Revisions: 2 times (View History)
Update Date: 06 Mar 2023
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