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. 2020 Sep 2;41(11):3149–3156. doi: 10.1007/s10072-020-04693-y

Table 2.

Characteristics of patients with GBS related to COVID-19 infection

Patient no. GBS symptoms Nerve studies
1 [30] • Paresthesia in feet and hands

• A flaccid severe tetraparesia

• Medical Research Council (MRC) strength evaluation was 2/5 in the legs, 2/5 the arms, 3/5 in the forearms and 4/5 in the hands

• Tendon reflexes were abolished in the four limbs

• Swallowing disturbance

2 [31]

• Asthenia, and myalgia in legs

• Paraesthesia, hypoesthesia, and distal weakness in the lower limbs

• Midthigh and tip of the fingers associated with ataxia

• Right peripheral facial palsy

• Decreased light touch from midthigh to feet and the tip of the fingers

• Decreased vibration sense in the lower limbs

• Symmetric weakness for dorsiflexion

• Extension of the toes (MRC score = 3/5) and flexion of the thigh (MRC = 4/5)

• Areflexia in the forelimbs apart from the left biceps reflex

3 [31] • acute proximal tetraparesis and distal forelimb and perioral paraesthesia.

• proximal lower limb weakness (MRC 2/5), distal weakness (MRC 4/5), and diffuse areflexia

• A typical demyelinating pattern with a conduction block in the left median nerve

• temporal dispersion, upper limb increased motor distal latencies

• Diffuse decreased motor and sensory conduction velocities

• Lower than 38 m/s in 9 nerves of 10 tested, and neurogenic pattern on EMG

• Left peripheral facial palsy

4 [32] • Symmetric weakness in lower limbs, leading to falls and paraplegia

• Weakness in the upper limbs (MRC 4/5) and diffuse areflexia, but no clear sensory deficits

• F-waves with diffuse prolonged distal motor latencies and reduced distal compound muscle action potential amplitudes with a slight reduction of conduction velocities, thus suggesting a mixed pattern of demyelination and axonal damage

• No sensory nerve action potential was registered

5 [33]

• Paresthesia at limb extremities

• Distal weakness rapidly evolving to a severe

• Flaccid tetraparesis

• Symmetric limb weakness (MRC score 3/5 at upper limbs and 2/5 at lower limbs)

• Hypoesthesia at the 4 limbs

• Absent deep tendon reflexes

• Severe paresthesia in both hands and feet

• Absence of both the sural nerve sensory nerve action potential (SAP) and the tibial nerve compound muscle action potential (CMAP)

6 [34]

• Asthenia and paresthesia at feet and hands

• Gait difficulties

• Symmetric distal upper and lower limbs weakness

• Loss of deep tendon reflexes

• Preserved light touch and pinprick sensation

7 [35]

• Bilateral lower limb pain

• Irritability

• Difficulty walking

• Loss of balance

• Unilateral peripheral facial and bulbar palsy

• Left facial droop

• Effacement of left nasolabial fold while smiling

• Inability to close the left eye

• Raise the left eyebrow or frown

• All consistent with Bell’s palsy

• The position sensation was decreased

• Deep tendon reflexes were absent

• Dysmetria and appendicular ataxia were present in all four limbs

8 [36] • Weakness in both legs and severe fatigue

• Symmetric weakness (MRC grade 4/5)

• Areflexia in both legs and feet

• Sensation to light touch and pinprick was decreased distally

9 [37] • Numbness and weakness of his lower extremities

• (MRC: 2/5 strength in his lower extremities with 3/5 in his upper extremities)

• Absence of deep tendon reflexes

• Ascending paralysis with supporting physical exam findings

10 [38]

• Gait disturbance

• Weakness in hip flexors

• Paresthesias of his hands and feet

• Proprioceptive sense at the toes

• Bilateral facial weakness

• Dysphagia

• Dysarthria

• Neck flexion weakness and inability to ambulate

11 [38]

• Paresthesia of his hands and feet

• Gait disturbance

• Initial examination revealed 3/5 shoulder shrug, 4−/5 hip and neck flexion

• Diminished vibration and proprioception at the toes

• Reflexes were 1+ in the arms and absent in the legs

• Unable to stand or ambulate independently

12 [39]

• Bilateral weakness and tingling

• Sensation in all four extremities

• quadriplegia, hypotonia, areflexia, and bilateral positive Lasègue sign

• reduction or absence of electrical potentials in both motor and sensory nerves in all four limbs

13 [40] • Bilateral facial nerve palsy • No other neurological findings at examination
14 [41]

• Paraparesis

• Distal allodynia

• Difficulties in voiding and constipation

• Bilateral lower limb flaccid paresis

• Absent deep tendon reflexes of the upper and lower limb

• Idiomuscular response to percussion of the muscle tibialis anterior

• Indifferent plantar reflexes

• No sensory deficit

15 [42]

• Pain and numbness in distal lower and upper

• Extremities progressive weakness in legs

• A mild peripheral facial

• Nerve palsy on the right side

• Muscles’ forces were 4/5 in distal and proximal lower extremities according to the MRC grading

• The upper extremities showed no weakness

• Deep tendon reflexes were absent in all four limbs

• Demyelinating polyneuropathy

16 [42]

• Ascending lower and upper

• Extremities weakness

• Paresthesia

• Decreased forces, MRC grade of 2/5 at proximal and 3/5 at distal lower limbs, and 4/5 in both arms

• Deep tendon reflexes were absent in both legs and decreased to 1+ in the upper extremities

17 [43]

• Symmetric paresthesias

• Ascending appendicular weakness

• Mental status and cranial nerves were normal

• Strength was 4/5 neck flexion, 3/5 proximal upper and lower extremities bilaterally

• Tendon reflexes were absent

• Sensation to light touch was diminished to wrists and

• knees bilaterally

18 [44] • Symmetric ascending quadriparesis

• weakness in four limbs with a MRC scale of 2/5 in proximal, 3/5 in distal of the upper extremities and 1/5 in proximal, 2/5 in distal of the lower extremities

• Deep tendon reflexes were absent

• Reduction in the vibration and fine touch sensation distal to the ankle joints and also bifacial nerve palsy

• No spine sensory level

• AMSAN form

19 [45]

• Unsteadiness and paraesthesia in both hands

• Bilateral facial nerve palsy, oropharyngeal weakness, and severe proximal tetraparesis

• Mild proximal tetraparesis 4/5 on the Medical Research Council (MRC) scale with global areflexia

• Touch, pinprick and proprioception were normal

20 [46]

• Root-type pain in all four limbs

• Weakness in his lower limbs

• Inferior bilateral facial paresis

• Paraparesis

• Left external rectus muscle with horizontal diplopia

• Global areflexia

• Acute demyelinating polyneuropathy

• Denervation

• Paresis of the left external rectus muscle with horizontal diplopia when looking to the left

21 [47]

• Perioral paresthesias, but no facial weakness

• Ataxic gait

• Flexor bilaterally

• Neuro-ophthalmologic examination revealed visual acuity of 20/b25 in both eyes

• Right internuclear ophthalmoparesis and right fascicular oculomotor palsy

22 [47] • Acute onset of diplopia

• Visual acuity of 20/25 in both eyes

• Severe abduction deficits in both eyes, and fixation nystagmus, with the upper gaze more impaired, all consistent with bilateral abducens palsy

• Deep tendon reflexes were absent

23 [48]

• Proximally pronounced

• Moderate symmetric paraparesis

• Progressive proximally pronounced paraparesis, areflexia, and sensory loss with tingling of all extremities
24 [49]

• Inferior bilateral facial paresis

• Paraparesis

• Arreflexia
25 [50]

• Progressive weakness

• Numbness of the lower extremities

• Mild dysarthria due to jaw weakness and bilateral, predominantly lower limb weakness, with 4−/5 strengths in knee and ankle flexor and extensor muscles, and 4−/5 in the left and 4+/5 in right hip flexor muscles by the Medical Research Council (MRC) scale

• Tendon reflexes were absent

26 [51] • Flaccid areflexic tetraplegia evolving to facial weakness, upper limb paresthesia and respiratory failure
27 [51] • Facial diplegia and generalized areflexia evolving to lower limb paresthesia with ataxia
28 [51] • Flaccid tetraparesis and facial weakness evolving to areflexia and respiratory failure
29 [51] • Flaccid areflexic tetraparesis and ataxia
30 [51] • Facial weakness, flaccid areflexic paraplegia, and respiratory failure
31 [52] • Acute progressive paresthesia of distal lower extremities evolving to the upper limbs leading to quardiparesthesia

• Facial paralysis and mildly dysarthric speech

• Deep tendon reflexes were generally absent

• Acute demyelinating polyneuropathy