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. 2017 Dec 9;141(3):e21. doi: 10.1093/brain/awx329

Table 1.

Clinical characteristics of POLR3A patients

Study ID F1-3 F1-5 F1-7 F1-8 F2-1 F3-1 F4-1 F5-1 F6-1 F7-1 F8-1 F9-1 F10-1 F11-1 F12-1 F13-1 F14-1 F15-1 F16-1 F16-2 F17-1 F18-1 F19-1 F20-1 F21-3 F22-6 F22-7 F23-3 F23-5
c.1909+ 22G>A Het Het Het Het Het Het Het Het Het Het Het Het Het Het Het Het Het Het Het Het Het Het Hom
Second mutation Q31* Q31* Q31* Q31* D372N F431Sfs*26 E1261K L454F S825Qfs*18 G904* A515V G854Afs*5 splice Q511* V1315fs*7 K713Kfs*3 C109S G350Gfs*27 R873* R873* M852fs*7 L356P V1033A (hom) c.1771-7C>G (hom)
Mode of inheritance AR AR AR AR AR S S S S AR S S S S S S S AR AR AR S S S ARa S AR AR AR AR
Gender F M F M F M M M M F M M F M M F F F F F M M F M M F F M F
Race CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU CAU
Origin GER GER GER GER GER GER GER GER GER USA UK GER GER GER GER GER GER GER UK UK UK UK USA BEL GER TR TR IL IL
Age at onset (y) 51 15 20 14 20 15 20 28 13 17 18 12 26 12 18 6 12 31 21 23 12 20 11 2 16 0b 0b 2 2
Age at exam (y) 57 53 50 48 47 68 56 38 27 30 31 42 56 66 41 50 45 45 30 35 25 42 18 20 55 29 21c 12 19
Loss of independent walkingd N/A 23 8 18 26 29 27 N/A N/A N/A 13 27 29 26 N/A 37 31 N/A 7 7 8 10 12 32 N/A 14 0e N/A 16
Cognitive deficits + +f + + +
Depression + + + + + + + + + + + +
Pyramidal and peripheral motor system
UL/LL spasticity −/− −/+ −/+ −/+ −/+ −/+ −/+ +/+ −/− −/+ −/+ −/+ −/+ −/+ −/+ −/− −/− −/+ −/+ −/+ −/+ −/+ −/− −/− −/+ −/− −/− −/− −/−
UL/LL tendon reflexes ↓/↓ ↔/↔ ↔/↑ −/↔ ↓/↓ −/− ↔/↓ ↔/↓ ↔/↓ ↔/↑ −/↓ ↔/↑ ↑/↔ ↑/↑ ↔/↓ −/↔ −/↓ ↔/↔ −/− −/− −/↔ −/↔ −/− ↔/↔ ↔/↔ ↔/↓ ↔/↓ ↔/↔ ↔/↔
Extensor plantar response + + + + + + + + + + + + + + + + +
UL/LL weakness −/− −/+ −/+ −/+ −/+ −/+ −/+ −/+ −/+ −/+ −/+ −/+ −/− −/+ −/+ −/+ −/+ −/+ −/+ −/+ +/+ +/+ −/+ −/− −/+ −/+ −/+ −/− −/+
Muscle atrophy LL LL UL/LL UL/LL LL UL/LL LL n.d. LL
Cerebellar system
Sacc. pursuit + + + + + + + + + + + + + + + + + + + +
Dysarthria/ dysphagia −/− +/− +/+ +/− +/− +/− −/− −/− −/− −/− −/− −/− −/− +/+ −/− −/− +/− −/− +/− +/− −/− +/− −/− +/− +/− +/+ +/+ +/+ +/+
UL/LL intention tremor +/− +/− −/− +/− +/− +/− +/− −/− −/− −/− −/− −/− −/− +/− −/+ +/− +/− −/+ +/− −/− +/+ −/− −/− +/+ +/+ −/− −/− −/− −/−
Ataxia + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Vibration/surface sens. (LL) ↓/↓ ↓/↓ ↓/↓ ↓/↓ ↓/↓ ↓/↓ ↓/↓ ↓/↓ ↓/↓ ↓/↔ ↓/↓ ↓/↔ ↓/↔ ↓/↔ ↓/↓ ↓/↓ ↓/↔ ↓/↔ ↓/↓ n.d. ↓/↓ n.d. ↓/↔ ↔/↔ ↓/↔ ↓/↔ ↓/↓ n.d. n.d.
Urinary/faecal urgency −/− +/− +/− +/− −/− −/− +/+ +/− −/− +/− −/− +/− +/n.d +/− +/− +/− +/− −/− −/+ −/+ −/− −/− −/− −/− +/− −/− +/+ −/− −/−
Dentition abnormalities + + + + + + + n.d. + n.d. n.d. + n.d. + + n.d. n.d. n.d. n.d. n.d.
Others RLS, sleep disturbance Facial hemispasm, sleep disturbance Sleep disturbance RLS, sleep disturbance Sleep disturbance RLS, sleep disturbance Aggressive behaviour Tremor (head, voice, UL) Tremor (head, voice) Severe dystonic tremor (head, voice) Mild dystonic tremor (head) Tremor (head), RLS, vitiligo Pes cavus Pes cavus Autism Rigor Pes cavus Infantile seizures dystonia Rigor, hypokinesia Rigor, hypokinesia
Neurophysiology
Abnormal nerve conduction studies + + + n.d. + + n.d. n.d. n.d. n.d. + n.d. n.d. n.d. n.d.
Abnormal MEPs + + + + + + + + + n.d. n.d. + + n.d. + + + + n.d. n.d. n.d. n.d. n.d. + n.d. n.d. n.d. n.d. n.d.
Abnormal SEPs + + + + + + + + n.d. n.d. + + + n.d. n.d. + + + n.d. n.d. n.d. n.d. n.d. + n.d. n.d. n.d. n.d. n.d.
Abnormal VEPs n.d. n.d. n.d. n.d. n.d. n.d. + + n.d. n.d. n.d. n.d. + n.d. n.d. n.d. n.d. n.d. n.d. n.d. n.d. n.d. + n.d. n.d. n.d. n.d. n.d.
MRI
Spinal cord atrophy + + + + + n.d. + + n.d. n.d. + n.d. + + + + + + n.d. n.d. n.d. n.d. n.d. n.d.g n.d. n.d. n.d. n.d.
Cerebellar atrophy n.d. n.d. n.d. n.d. + n.d. n.d. n.d.
TCC + + + + + n.d. N/E n.d. N/E + N/E N/E N/E N/E N/E N/E + n.d. n.d. n.d.
SCP hyperintensity (FLAIR) + + + + + n.d. + + + N/E n.d. N/E + n.d. + + N/E N/E N/E N/E N/E N/E N/E n.d. n.d. n.d.
Hypomyelinaton n.d. n.d. n.d. n.d. n.d. n.d. n.d. n.d. n.d.

AR = autosomal recessive; BEL = Belgium; CAU = Caucasian; F = female; gen = generalized; GER = Germany; IL = Israel; LL = lower limb; M = male; MEP = motor evoked potential; n.d. = not done; N/E = not evaluated; RLS = restless legs syndrome; S = sporadic; SCP = superior cerebellar peduncle; SEP = cortical latencies of somatosensory evoked potentials; TCC = thin corpus callosum; TR = Turkey; UL = upper limb; VEP = cortical latencies of visual evoked potentials. + = clinical sign is present; − = clinical sign is absent; ↑ = increase of clinical sign; ↓ = decrease of clinical sign; ↔ = normal/unchanged findings.

aChild from incestuous relationship between brother and sister.

bStart at ∼2 months of age.

cDeath at age 24 years.

dIn years after disease onset.

eNever able to walk independently.

fSevere cognitive decline at the age of 39 years.

gAtrophy of brainstem and pons.