Case Reports in Genetics

Volume 2014 (2014), Article ID 691515, 5 pages

http://dx.doi.org/10.1155/2014/691515

Case Report

Alsin Related Disorders: Literature Review and Case Study with Novel Mutations

Filipa Flor-de-Lima,1,2 Mafalda Sampaio,³ Nahid Nahavandi,⁴ Susana Fernandes,⁵ and Miguel Leão3,5

¹Department of Pediatrics, Hospital Pediátrico Integrado, Centro Hospitalar de São João, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal

²Faculty of Medicine, University of Porto, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal

³Unit of Pediatric Neurology, Hospital Pediátrico Integrado, Centro Hospitalar de São João, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal

⁴Centogene AG, Schillingallee 68, 18057 Rostock, Germany

⁵Department of Genetics, Faculty of Medicine, University of Porto, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal

Received 31 May 2014; Revised 20 August 2014; Accepted 1 September 2014; Published 14 September 2014

Academic Editor: Patrick Morrison

Copyright © 2014 Filipa Flor-de-Lima et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Mutations in the ALS2 gene cause three distinct disorders: infantile ascending hereditary spastic paraplegia, juvenile primary lateral sclerosis, and autosomal recessive juvenile amyotrophic lateral sclerosis. We present a review of the literature and the case of a 16-year-old boy who is, to the best of our knowledge, the first Portuguese case with infantile ascending hereditary spastic paraplegia. Clinical investigations included sequencing analysis of the ALS2 gene, which revealed a heterozygous mutation in exon 5 (c.1425_1428del p.G477Af19) and a heterozygous and previously unreported variant in exon 3 (c.145G>A p.G49R). We also examined 42 reported cases on the clinical characteristics and neurophysiological and imaging studies of patients with known ALS2 gene mutations sourced from PubMed. This showed that an overlap of phenotypic manifestations can exist in patients with infantile ascending hereditary spastic paraplegia, juvenile primary lateral sclerosis, and juvenile amyotrophic lateral sclerosis.

1. Introduction

Three apparently distinct disorders involving retrograde degeneration of the upper motor neurons of the pyramidal tracts seem to be caused by mutations in the ALS2 gene, which provides instructions for making a protein called Alsin. They comprise a clinical continuum from infantile ascending hereditary spastic paraplegia (IAHSP) (OMIM number 607225), to juvenile forms without lower motor neuron involvement, namely, juvenile primary lateral sclerosis (JJPLS) (OMIM number 606353), and to forms with lower motor neuron involvement, namely, autosomal recessive juvenile amyotrophic lateral sclerosis (JALS) (OMIM number 205100) [1, 2]. There is no available data on the prevalence of ALS2 related disorders. However, they are probably currently underdiagnosed, even if they have been described in individuals from a variety of ethnic backgrounds, mainly from the Mediterranean [1].

All the patients are homozygous or heterozygous compounds for ALS2 mutations [1]. To date, a total of 45 patients with known mutations in the ALS2 gene have been described, but the phenotype-genotype correlation remains unclear [2]. In the present study, we describe the clinical and genetic features of a 16-year-old boy with IAHSP from Northern Portugal (Table 1).

Table 1: Mutations in ALS2 related disorders.

Patient
Exon/intron
Mutation
Predicted protein
Phenotypic classification
References

1
Intron 24
c.3836+1G>T
p.k1234fs*3
IAHSP
Racis et al., 2014 [5]

2
Intron 9
c.2000-2A>T
p.E724fs*32
IAHSP
Herzfeld et al., 2009 [6]

3
Exon 9
c.1825_1826ins5
p.E609fs*9
IAHSP
Sztriha et al., 2008 [7]

4
Exon 13
c.2529G>T
p.G1177*
IAHSP

5, 6
Exon 10
c.2143C>T
p.Q715*
IAHSP
Verschuuren-Bemelmans et al., 2008 [8]

7, 8
Exon 4
c.467G>A
p.C156Y
IAHSP
Eymard-Pierre et al., 2006 [9]

9, 10
Exon 18
c.2992C>T
p.R998*
IAHSP
Devon et al., 2003 [10]

11
Exon 32
c.4844delT
p.I331fs335
IAHSP
Gros-Louis et al., 2003 [11]

12–17
Exon 4
c.1130delAT
p.I331fs335
IAHSP
Eymard-Pierre et al., 2002 [12]

Exon 13
c.2660delAT
p.N845fs858
IAHSP

Exon 6
c.1471_1480del10
p.V491Gfs*3
IAHSP

Exon 22
c.3742delA
p.M1206*
IAHSP

18–20
Exon 5
C.1548delAG
p.T475Tfs*70
IAHSP
Hadano et al., 2001 [4]

21
Exon 5

Exon 3
c.1427_1428del

c.145G>A
p.G477Afs*19

p.G49R
IAHSP
Our study

22-23
Exon 4

Exon 14
c.299G>T

c.2580-2A>G
p.S100I
JALS

JALS
Luigetti et al., 2013 [13]

24-25
Exon 22
c.3565delG
p.V1189WfsX19
JALS
Shirakawa et al., 2009 [2]

26
Exon 4
c.553delA
p.T185LfsX5
JALS
Kress et al., 2005 [14]

27–38
Exon 3
c.138delA
p.A46AfsX5
JALS
Hadano et al., 2001 [4]

39–41
Intron 17
c.2980-A>G
p.T993fs*7
JPLS
Mintchev et al., 2009 [15]

42
Exon 6
c.1619G
p.G540E
JPLS
Panzeri et al., 2006 [16]

2. Case Report

The patient was born after a twin pregnancy from nonconsanguineous parents and the pregnancy included maternal hemorrhage in the second trimester. Delivery was at the 36th week of gestation by Cesarean section. The twins were dizygotic twins and the patient’s twin sibling is healthy. His 42-year-old mother is healthy and his father died at the age of 35 after a car accident, without any signs of a neurological disorder. The boy acquired cephalic control at three months and started to sit unaided at six months, crawl at nine months, and walk with support at 10 to 11 months. Stiffness of the lower limbs and tiptoeing with hyperactive deep tendon reflexes were noticed at the age of three and scissoring gait started during his fourth year. He was never able to walk without support and underwent Achilles tenotomy at the ages of three and five. An ascending progression of motor difficulties was observed, with spasticity becoming evident in the upper extremities after the age of six. Muscle atrophy in the lower limbs was evident after the age of seven and he was wheelchair bound at the age of eight. Sphincter incontinence started at the same time and he developed supranuclear bulbar palsy, with progressive dysarthria. MRI, electromyography, and nerve conduction studies at that age were normal. Anarthria was evident at the age of 13. At the age of 14, there was clinical worsening and since then he has had bilateral limitation of horizontal eye movements, dysphagia when drinking liquids, chewing difficulties, severe drooling, and paroxysms of laughter. Cognitive function is still normal at the age of 16.

3. Material and Methods

DNA was extracted from a peripheral blood sample from the patient, his mother, and twin brother. All 34 exons of the ALS2 gene were analysed by PCR and sequencing of both DNA strands of the entire coding region was carried out, including the highly conserved exon-intron splice junctions.

We also reviewed all cases of ALS2 related disorders with known ALS2 gene mutations and detailed clinical, neurophysiological, and imaging data that have so far been reported in PubMed. Continuous variables with asymmetric distribution are described by medians (minimum to maximum) and categorical variables are described by absolute and relative frequencies. To compare the three phenotypes (IAHSP, JALS, and JPLS) we used the Kruskal-Wallis test if the variables were continuous and the Monte Carlo test if they were categorical. The statistical analysis was performed using SPSS v.20 (IBM, USA) and values of less than 0.05 were considered significantly different.

4. Results and Discussion

Our patient displays a clinical picture that is highly suggestive of ALS2 related disorder. This case study presents evidence of previously unreported heterozygous variants in exon 5 (c.1425_1428del p.G477Af19) and exon 3 (c.145G>A p.G49R).

To date, case studies of 45 patients with ALS mutations have been reported. Four patients with JALS were excluded because a detailed clinical description was not available [3]. The clinical characteristics and neurophysiological and imaging studies of the remaining 41 cases, plus our case study, are summarized in Table 2. Of these, 21 (50%) of the patients were classified as having an IAHSP phenotype, 17 (40.5%) had a JALS phenotype, and four (9.5%) had a JPLS phenotype. Median age at onset of walking loss, upper limb involvement, speech impairment, and becoming wheelchair bound was similar between the three groups.

Table 2: Summary of the characteristics of 42 patients with known ALS2 gene mutations.

Patient
Age
Origin
Motor development by 1 year
Age at onset
Loss of walking
Upper limb involvement
Bulbar involvement
Speech impairment
Ocular movements
Wheelchair bound
EMG
Evoked potentials
Brain imaging
Phenotypic classification
References

1
17 y
Italy
Ab
12 mo
NA
8 y
8 y
Disarthria at 8 y, Anarthria at 11 y

8 y
Ab
SSEP ab
Ab
IAHSP
Racis et al., 2014 [5]

2
7 y
Germany
Ab
18 mo
<7 y
<7 y
7 y

N
7 y

Ab
IAHSP
Herzfeld et al., 2009 [6]

3
11 y
Hungary
Ab
10 mo
NA
2 y
5 y
No
N
11 y
N
Motor ab
N
IAHSP
Sztriha et al., 2008 [7]

4
6 y
Hungary
Ab
<1 y
NA
No
5 y
No
N
5 y

N
IAHSP

5
13 y
The Netherlands
Ab
8 mo
NA
3 y
5 y
Anarthria at 13 y
N
13 y
N
MEP Unobtainable
N
IAHSP
Verschuuren-Bemelmans et al., 2008 [8]

6
8 y
The Netherlands
Grossly N
18 mo
NA
Yes
4 y
No
N
No
N
MEP Unobtainable
N
IAHSP

7
22 y
Turkey
Ab
1 y
12 y
12 y
16 y
No

12 y

IAHSP
Eymard-Pierre et al., 2006 [9]

8
20 y
Turkey
Ab
1 y
10 y

12 y
No

10 y
N
Motor ab
Ab
IAHSP

9
9 y
Bukhari Jewish
N
1-2 y
NA
2 y
3 y
Dysarthria at 9 y

No

IAHSP
Devon et al., 2003 [10]

10
6 y
Bukhari Jewish
N
14 mo
6 y
6 y
6 y
Dysarthria at 6 y

No
N

N
IAHSP

11
12 y
Pakistan
Ab
18 mo
12 y

<12 y
Anarthria at 12 y

12 y

IAHSP
Gros-Louis et al., 2003 [11]

12
36 y
Algeria

1 y
NA
<7 y
13 y
Dysarthria at 13 y
N

N
MEP and SSEP abnormal
Ab
IAHSP

Eymard-Pierre et al., 2002 [12]

13
31 y
Algeria

1 y
NA
<7 y
13 y
Dysarthria at 13 y
N

N
MEP and SSEP abnormal

IAHSP

14
24 y
Algeria

1 y
NA
<7 y
13 y
Dysarthria at 13 y
N

N
MEP and SSEP abnormal

IAHSP

15
18 y
France

1.5 y
4 y
6 y
8 y
Dysarthria at 4 y, anarthria at 12 y
Ab

N
MEP and SSEP abnormal
Ab
IAHSP

16
23 y
Italy

1.4 y
5 y
10 y
12 y
Dysarthria at 10 y, anarthria at 16 y
Ab

N
MEP and SSEP abnormal
Ab
IAHSP

17
20 y
Italy

1.5 y
4 y
9 y
13 y
Dysarthria at 11 y, anarthria at 18 y
Ab

N
MEP and SSEP abnormal
Ab
IAHSP

18
14 y
Kuwait
N
14 mo
2 y
9 y
4 y
Dysarthria at 4 y, anarthria at 14 y

N
N
Ab
IAHSP
Hadano et al., 2001 [4]

19
6 y
Kuwait
Ab
11 mo
NA

5 y
Dysarthria at 5 y,
N
No

Ab
IAHSP

20
2 y
Kuwait
Ab
9 mo
NA

IAHSP

21
16 y
Portugal
N
3 y
NA
6 y
8 y
Dysarthria at 8 y, anarthria at 13 y
Ab
8 y
N

N
IAHSP
Our study

22
27 y
Italy
N
3 y

Dysarthria at 7 y, anarthria at 14 y

Ab
SSEP N
N
JALS
Luigetti et al., 2013 [13]

23
21 y
Italy
N
6 y

Ab
SSEP N
N
JALS

24
32 y
Japan
N
13 mo
No

11 y
Dysarthria at 11 y, anarthria at 14 y

No
Ab

N
JALS
Shirakawa et al., 2009 [2]

25
23 y
Japan
N
3 y
No

Dysarthria

No

JALS

26
32 y
Turkey
Ab
22 mo
16 y
12 y
15 y
18 y

16 y
Ab
Motor ab, SSEP N

JALS
Kress et al., 2005 [14]

27
60 y
Tunisia
N
10 y

10 y

N
Motor N

JALS
Hadano et al., 2001 [4]

28
36 y
Tunisia
N
6.5 y

6.5 y

N

JALS

29
27 y
Tunisia
N
3.5 y

Yes

N
Motor N, SSEP ab

JALS

30
22 y
Tunisia
N
6.5 y

6.5 y

N
Motor N

JALS

31
21 y
Tunisia
N
9 y

9 y

N

JALS

32
14 y
Tunisia
N
6.5 y

6.5 y

N

JALS

33
23 y
Tunisia
N
6.5 y

6.5 y

N
Motor N

JALS

34
28 y
Tunisia
N
3.5 y

Yes

N

JALS

35
32 y
Tunisia
N
7.5 y

Yes

N
Motor N

JALS

36
22 y
Tunisia
N
6.5 y

Yes

N

JALS

37
21 y
Tunisia
N
10 y

Yes

N
Motor N, SSEP ab

JALS

38
7 y
Tunisia
N
6 y

Yes

N

JALS

39
55 y
Cyprus
N
2 y
50 y
Yes
3 y

Ab
50 y

JPLS
Mintchev et al., 2009 [15]

40
42 y
Cyprus
N
2 y
2 y
Yes
2 y

Ab
2 y

SSEP N
N
JPLS

41
16 y
Cyprus
N
2 y
No
Yes
2 y

Ab
No
Ab

JPLS

42
34 y
Italy
N
2 y
19 y
2 y
6 y
Dysarthria at 6 y, anarthria at 20 y
Ab
34 y
Ab
Motor ab
N
JPLS
Panzeri et al., 2006 [16]

EMG: electromyography; N: normal; Ab: abnormal; NA: not achieved; y: years; mo: months; MEP: motor evoked potentials; SSEP: somatosensory evoked potentials.

The heterozygous variant in exon 5 (c.1425_1428del p.G477Af19) creates a shift in the reading frame, starting at codon 477. The new reading frame ends in a stop codon 18 positions downstream, which is very likely to result in truncated protein or loss of protein production. Therefore, it is very likely to be a disease causing mutation. A small deletion in this region (c.1427_1428delAG), which also causes a frameshift, has previously been described as disease causing for ALS2 [4]. The other unreported heterozygous variant was found in exon 3 (c.145G>A p.G49R), which is located in a moderately conserved amino acid, with moderate physiochemical differences between the amino acids glycine and arginine. Polyphen-2, SIFT, and MutationTaster predict that this variant is probably damaging. This variant in exon 3 was also found in our patient’s twin brother and their mother, who were both healthy. It was impossible to test his father because he was dead.

Despite the limited number of patients reported in the literature with known ALS2 mutations and considering the bias related to the age, the majority of clinical characteristics were similar between both groups. Because all the families reported to date have had different ALS2 mutations, it is impossible to draw any genotype-phenotype correlation.

5. Conclusions

Despite the limited information about clinical characteristics, patients with IAHSP, JALS, and JPLS may present with different phenotypes that overlap.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

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