Table 4 Summary of clinical information.

From: Less common phenotypes of myelin oligodendrocyte glycoprotein antibody-related diseases in children deserve more attention

 

Cortical encephalitis

MNOS

Cerebral leukodystrophy -like phenotype

Isolated seizures

Aseptic meningitis

Median age, years

9.1

11

5.3

10.3

4.3

Clinical presentation

 Seizures

88.9

92.3

42.9

100

33.3

 Headache

72.2

76.9

42.9

0

66.7

 Fever

61.1

38.5

28.6

0

100

 Motor disorder

38.9

84.6

57.1

0

33.3

 Cognitive dysfunction

27.8

76.9

42.9

0

33.3

 Abnormal (psychiatric) behavior

0

84.6

0

0

0

 consciousness disturbance

38.9

76.9

42.9

0

66.7

 Sleep disorder

0

61.5

0

0

0

CSF WBC increase

66.7

46.2

42.9

33.3

100

MRI

Cortical hyperintensities 100

Supratentorial 100

infratentorial 61.5

Subcortical

white matter 100

Normal

Non-specificity 66.7

meningeal enhancement33.3

Misdiagnosis

Viral Encephalitis62.5

Epilepsy 18.8

Purulent meningitis6.2

Cerebral stroke 6.2

ON 15.4

CCE 15.4

NMADR-E 15.4

ADEM 85.7

Epilepsy 66.7

Viral Encephalitis 33.3

Purulent meningitis 66.7

Viral Encephalitis 33.3

Time to first immunotherapy Median, days

14 (IQR: 7.5–20)

15 (IQR: 8–22)

15 (IQR: 11–22)

/

19 (IQR: 8–23)

Type of immunotherapy given

 IVIg+HIMP

37.5

38.5

100

0

66.7

 IVIg

18.8

7.7

0

0

33.3

 HIMP

0

7.7

0

0

0

 Relapse

68.8

84.6

50

66.7

0

  1. Numbers are expressed as percentages.
  2. MNOS overlapping syndrome of MOGAD and anti-N-methyl-D aspartate receptor encephalitis, CSF cerebrospinal fluid, MRI magnetic resonance imaging, IVIg Intravenous immunoglobulins, HIMP High doses of intravenous methylprednisolon.