Table 1 Main clinical findings in NAA60-related disease

From: Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications

Family

1

1

2

2

3

3

4

5

6

7

Individual

F1-II-1

F1-II-2

F2-II-2

F2-II-1

F3-II-1

F3-II-2

F4-II-1

F5-II-1

F6-II-6

F7-II-6

Origin of case

UK

UK

France/Algeria

France/Algeria

France/Morocco

France/Morocco

UK/India (Gujarati)

Turkey

Turkey

Saudi Arabia

Consanguinity

No

No

Yes

Yes

Yes

Yes

No

Yes

Yes

Yes

cDNA sequence

c.321_327del

c.321_327del

c.338-1 G > C

c.338-1 G > C

c.338-1 G > C

c.338-1 G > C

c.391 C > T

c.130 C > T

c.50 T > G

c.428 A > C

Amino-acid change

(p.Arg108Thrfs*3)

(p.Arg108Thrfs*3)

p.(Gly113Valfs*32)

p.(Gly113Valfs*32)

p.(Gly113Valfs*32)

p.(Gly113Valfs*32)

(p.His131Tyr)

(p.Arg44Cys)

(p.Leu17Arg)

(p.Asn143Thr)

Zygosity

Homozygous

Homozygous

Homozygous

Homozygous

Homozygous

Homozygous

Homozygous

Homozygous

Homozygous

Homozygous

Age of onset

Early twenties

Early twenties

Early thirties

Developmental delay from birth. Onset motor symptoms at age 20

Mild intellectual disability from birth. Onset of motor symptoms at age 31

Mild intellectual disability from birth. Onset of motor symptoms at age 24

Mild symptoms at birth. Onset of motor symptoms at age 10

Developmental delay from birth.

Developmental delay from birth.

Late twenties

Motor features and movement disorders

Extrapyramidal and cerebellar syndrome

Extrapyramidal and cerebellar syndrome

No

Extrapyramidal and cerebellar syndrome, dystonia

Pyramidal and cerebellar syndrome

Pyramidal, extrapyramidal and cerebellar syndrome

Hypotonia, tics and stereotypies, tongue dyskinesia, dystonia, chorea, and pyramidal syndrome

Pyramidal syndrome, dystonia

Pyramidal syndrome

Pyramidal and cerebellar syndrome.

Psychiatric features

No

Psychosis. schizophrenia

No

No

Mild intellectual disability, depression, anxiety

Mild intellectual disability

ADHD

No

Mild intellectual disability, ADHD

No

Cognitive features

Cognitive impairment

Cognitive impairment

Mild frontal syndrome

Learning difficulties

Mild learning difficulties

Mild learning difficulties

Learning difficulties

Delayed language development

Mild learning difficulties

Mild cognitive impairment

Disease duration at last examination

17 years

15 years

6 years

47 years

39 years

33 years

6 years

9 years

12 years

2 months

Findings at the last examination

Severe cerebellar syndrome and parkinsonism, anarthria, unable to swallow

Anarthria, severe parkinsonism, unable to swallow

Unremarkable

Cerebellar syndrome, parkinsonism, dystonia

Pyramidal and cerebellar syndrome, Mild intellectual disability, depression, anxiety

Pyramidal syndrome, mild parkinsonism, moderate cerebellar ataxia

NA

Pyramidal syndrome, delayed motor milestones, dystonia, quadriparesis

Pyramidal syndrome

Pyramidal and cerebellar syndrome