Case Report

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

Table 2

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

PatientAgeOriginMotor development by 1 yearAge at onsetLoss of walkingUpper limb involvementBulbar involvementSpeech impairmentOcular movementsWheelchair boundEMGEvoked potentialsBrain imagingPhenotypic classificationReferences

117 yItalyAb12 moNA8 y8 y Disarthria at 8 y, Anarthria at 11 y8 yAbSSEP abAbIAHSPRacis et al., 2014 [5]

27 yGermanyAb18 mo<7 y<7 y7 yN7 yAbIAHSPHerzfeld et al., 2009 [6]

311 yHungaryAb10 moNA2 y5 yNoN11 yNMotor abNIAHSP Sztriha et al., 2008 [7]
46 yHungaryAb<1 yNANo5 yNoN5 yNIAHSP

513 yThe NetherlandsAb8 moNA3 y5 yAnarthria at 13 yN13 yNMEP UnobtainableNIAHSP Verschuuren-Bemelmans et al., 2008 [8]
68 yThe NetherlandsGrossly N18 moNAYes4 yNoNNoNMEP UnobtainableNIAHSP

722 yTurkeyAb1 y12 y12 y16 yNo12 yIAHSP Eymard-Pierre et al., 2006 [9]
820 yTurkeyAb1 y10 y12 yNo10 yNMotor abAbIAHSP

99 yBukhari JewishN1-2 yNA2 y3 yDysarthria at 9 yNoIAHSP Devon et al., 2003 [10]
106 yBukhari JewishN14 mo6 y6 y6 yDysarthria at 6 yNoNNIAHSP

1112 yPakistanAb18 mo12 y<12 yAnarthria at 12 y12 yIAHSPGros-Louis et al., 2003 [11]

1236 yAlgeria1 yNA<7 y13 yDysarthria at 13 yNNMEP and SSEP abnormalAbIAHSP












Eymard-Pierre et al., 2002 [12]
1331 yAlgeria1 yNA<7 y13 yDysarthria at 13 yNNMEP and SSEP abnormalIAHSP
1424 yAlgeria1 yNA<7 y13 yDysarthria at 13 yNNMEP and SSEP abnormalIAHSP
1518 yFrance1.5 y4 y6 y8 yDysarthria at 4 y, anarthria at 12 yAbNMEP and SSEP abnormalAbIAHSP
1623 yItaly1.4 y5 y10 y12 yDysarthria at 10 y, anarthria at 16 yAbNMEP and SSEP abnormalAbIAHSP
1720 yItaly1.5 y4 y9 y13 yDysarthria at 11 y, anarthria at 18 yAbNMEP and SSEP abnormalAbIAHSP

1814 yKuwaitN14 mo2 y9 y4 yDysarthria at 4 y, anarthria at 14 yNNAbIAHSP Hadano et al., 2001 [4]
196 yKuwaitAb11 moNA5 yDysarthria at 5 y,NNoAbIAHSP
202 yKuwaitAb9 moNAIAHSP

2116 yPortugalN3 yNA6 y8 yDysarthria at 8 y, anarthria at 13 yAb8 yNNIAHSPOur study

2227 yItalyN3 yDysarthria at 7 y, anarthria at 14 yAbSSEP NNJALS Luigetti et al., 2013 [13]
2321 yItalyN6 yAbSSEP NNJALS

2432 yJapanN13 moNo11 yDysarthria at 11 y, anarthria at 14 yNoAbNJALS Shirakawa et al., 2009 [2]
2523 yJapanN3 yNo DysarthriaNoJALS

2632 yTurkeyAb22 mo16 y12 y15 y18 y16 yAbMotor ab, SSEP NJALSKress et al., 2005 [14]

2760 yTunisiaN10 y10 yNMotor NJALS Hadano et al., 2001 [4]
2836 yTunisiaN6.5 y6.5 yNJALS
2927 yTunisiaN3.5 yYesNMotor N, SSEP abJALS
3022 yTunisiaN6.5 y6.5 yNMotor NJALS
3121 yTunisiaN9 y9 yNJALS
3214 yTunisiaN6.5 y6.5 yNJALS
3323 yTunisiaN6.5 y6.5 yNMotor NJALS
3428 yTunisiaN3.5 yYesNJALS
3532 yTunisiaN7.5 yYesNMotor NJALS
3622 yTunisiaN6.5 yYesNJALS
3721 yTunisiaN10 yYesNMotor N, SSEP abJALS
387 yTunisiaN6 yYesNJALS

3955 yCyprusN2 y50 yYes3 yAb50 yJPLS Mintchev et al., 2009 [15]
4042 yCyprusN2 y2 yYes2 yAb2 ySSEP NNJPLS
4116 yCyprusN2 yNoYes2 yAbNoAbJPLS

4234 yItalyN2 y19 y2 y6 yDysarthria at 6 y, anarthria at 20 yAb34 yAbMotor abNJPLSPanzeri 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.