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Table 1 The clinical summary of GD patients whose EEG monitoring had neuronopathic features

From: Electroencephalogram and phenotype patterns in neuronopathic Gaucher disease patients – ten years of experience in a single center

Pt’s No

Age at time of EEG

GD type

Seizure types

Eye findings

Other neurological symptoms

Major EEG abnormities

HSNP

STR

Awake

Discharges

Sleep

1

13y

7mo

3

Myoclonic

Tonic-clonic

(-)

(-)

Ataxia

+

+

Polyspike and wave, spike rhythm

2

8y

4mo

3

Tonic-clonic

Tonic

(-)

+

(-)

+

+

(Poly)spike and wave, ESES

3

16y

11mo

3

Myoclonic

(-)

(-)

Parkinsonian tremor

+

+

Polyspike and wave

4

19y

9mo

3

Tonic-clonic

(-)

(-)

(-)

+

+

(Poly)spike and wave

5

8mo

2

Tonic

(-)

(-)

Developmental delay

(-)

+

Spike and wave

6

5y

2mo

3

Tonic-clonic Clonic

+

+

Ataxia, Developmental delay, Parkinsonian tremor

+

+

(Poly)spike and wave

7

20y

2mo

3

Tonic

(-)

(-)

(-)

+

+

(Poly)spike and wave

8

7y

10mo

3

Tonic-clonic

(-)

(-)

Ataxia

+

+

Spike and wave

9

8y

11mo

3

Tonic

(-)

(-)

Developmental delay

+

+

(Spike)sharp and wave

10

9y

4mo

3

(-)

(-)

+

Developmental delay, Parkinsonian tremor

+

+

Spike and wave

11

6y

3

(-)R

+

(-)

Ataxia

+

+

(Poly)spike and wave

12

4y

3

(-)

+

+

(-)

(-)

+

Spike and wave

13

11y

10mo

1

(-)R

(-)

(-)

(-)

+

+

Polyspike and wave, spike rhythm

14

11y

11mo

1

(-)R

(-)

(-)

(-)

+

NREM I

Spike and wave

15

8y

1

(-)

(-)

(-)

(-)

+

+

Sharp and wave

  1. HSNP Horizontal supranuclear palsy, ophthalmoplegia, STR Strabismus, NREM I Non-rapid eye movement stage I, R initial seizure episodes were reported when composing this article, (-) Abscent