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. 2019 Apr 25;14:83. doi: 10.1186/s13023-019-1053-1

Table 1.

Literatures review of reported HSP patients with CAPN1 mutations

Study (year) Case No. Gender Population Consanguinity Mutations Het/Hom Exon Transcript Age at onset (year) Clinical features MR or CT imaging (Brain or spine)
Lower limbs spasticity Lower limbs hyperreflexia Upper limbs hyperreflexia Babinski sign Skeletal or tendon deformity Weakness or amyptrophy Ocular movement disorder Abnormal bladder function Dysarthria Ataxia Additional symptoms
Gan-Or Z, et al. (2016) [7] 3 M Mornoccan Y C.884G > C (p.R295P) Hom exon8 NM_005186 NA NA NA NA NA NA NA NA NA NA NA NA NA
F 20 + + + + + + + + NA NA
F NA NA NA NA NA NA NA NA NA NA NA NA NA
5 M Mornoccan Y C.1579C > T (p.Q527*) Hom exon14 35 + + + + + + hypoesthesia, peripheral, neuropathy, dysarthria, akinetic face, abolished sympathetic skin reflex in lower limbs NA
F 36 + + + + + + + + peripheral neuropathy, facial hypokinesia, abolished sympathetic skin reflex in lower limbs NA
M 22 + + + + + + + NA
M 39 + + + + + + NA NA
F 24 + + + + + + abolished sympathetic skin reflex in lower limbs NA
2 M Ladho and Utah N C.406delC (p.P136Rfs*40)
c.1605 + 5 G > A
Com-het exon4
exon14
33 + NA NA + + NA NA NA mild atrophy of cervical spinal cord
F 19 + + + + + + + NA + NA slightly prominent sulci
Wang Y, et al. (2016) [11] 2 F Bangladeshi Y c.337 + 1 G > A Hom exon3 NM_001198868 Late teens + + NA NA NA NA NA NA + + dysphagia, mild cognitive decline mild cerebellar atrophy
F NA NA NA NA NA NA NA NA NA NA NA NA
1 F Italian NC c.183dupC (p.F61 fs) Hom exon2 25 + + + + NA NA NA + + + dysphagia, bilateral positive Hoffmann’s reflex
2 F Tunisian Y c.1534C > T (p.R512C) Hom exon13 23 + + + NA NA NA NA + + NA cerebellar atrophy
F 20 + + + NA NA NA NA + + NA NA
1 F French Y c.463C > T (p.Q155X)
c.1142C > T (p.A381V)
Com-het exon5
exon10
20 + + + + + + + + + + dysphagia, hypokinesia, vibration sense at ankles decreased,
bilateral positive Hoffmann’s reflex
cerebellar atrophy, white matter changes, mild vermian atrophy
Travaglini,L, et al. (2017) [12] 1 M Italian N c.221G > A (p.G74D)
c.911C > T (p.T304 M)
c.1418G > T (p.R473L)
Com-het exon2
exon8
exon13
NM_001198868 5 + + NA + NA NA NA NA NA NA spastic hypertonia
Tadic V, et al. (2017) [13] 2 F NA Y c.759 + 1 G > A Hom exon6 NM_001198868 29 + + NA + + NA + NA + + muscle hypertonic cerebellar vermal atrophy
F 33 NA + NA ± + NA NA NA NA + slight intention tremor NA
Kocoglu C, et al. (2018) [15] 1 F NA NA c.994G > A (p.G332R) Hom exon9 NM_001198868 21 + NA NA NA + + NA NA + + upper limb spasticity keratoconus
2 F NA Y c.1176G > A (P.R392*) Hom exon10 15 + + NA + + NA NA NA + + upper limb spasticity
F 15 + + NA + NA NA NA NA + + NA NA
Lambe J, et al. (2018) [14] 1 F Irish N c.1534C > T (p.R512C) Hom exon13 NM_001198868 14 + + + + NA NA NA + NA midbrain pons, cerebellar atrophy, spinal cord normal
Shetty A, et al. (2018) [16] 1 F Japanese Y c.2118 + 1G > T Hom exon21 NA 37 NA NA NA NA NA NA NA NA NA + upper motor neuron findings in the legs NA
2 M Turkish Y c.397C > T Hom exon4 NA 23 NA NA NA NA NA NA NA NA NA NA progressive spastic paraparesis NA
F NA 20 NA NA NA NA NA NA NA NA NA NA severe proximal weakness NA
1 M Punjabi Y c.843 + 1G > C Hom exon7 NA 37 + NA NA NA NA NA NA NA NA + spastic quadriparesis NA
Melo US. et al. (2018) [17] 3 F Brazilian Y c.1176G > A (P.R392*) Hom exon10 NM_001198868 NA + NA NA NA NA NA NA NA + two of three NA NA
F NA + NA NA NA NA NA NA NA + NA NA
M NA + NA NA NA NA NA NA NA + NA NA
1 F Y c.1176G > A (P.R392*) Hom exon10 22 + + NA NA NA NA NA NA NA NA NA
2 F Y c,675C > A p.Y225* Hom eoxn6 20 + NA NA NA NA NA NA NA NA + NA NA
M 35 + NA NA NA NA NA NA NA NA + NA NA
2 F N c.1176G > A (P.R392*)
c.618_619 delAG (p.G208 Qfs*7)
Com-het exon10
exon6
30 + NA NA NA NA NA NA NA NA + NA NA
M Y c.1176G > A (p.R392*) Hom exon10 38 + NA NA NA NA NA NA NA NA + NA NA
Current study 2 M Chinese Y c.142C > T (p.R48*) Hom exon2 NM_001198868 18 + + + + NA muscle hypertonic in lower limbs, bilateral positive Hoffmann’s reflex
F Y c.1015C > T (p.R339X) Hom exon10 41 + + + + + bilateral positive Hoffmann’s reflex

AR autosomal-recessive, com-het compound heterozygous, CT computed tomography, hom homozygous, HSP Hereditary Spastic Paraplegia, F female, M male, MRI magnetic resonance image, N no, NA not available, NC not certain, Y yes, y years old, +: positive, −: negative or normal, ±:suspicious