Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene

Eleonore Eymard-Pierre, Gaetan Lesca, Sandra Dollet, Filippo Maria Santorelli, Matteo Di Capua, Enrico Bertini, Odile Boespflug-Tanguy

Research output: Contribution to journalArticle

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Abstract

We studied 15 patients, from 10 families, who presented with severe spastic paralysis with an infantile onset and an ascending progression. Spastic paraplegia began during the first 2 years of life and extended to upper limbs within the next few years. During the first decade of life, the disease progressed to tetraplegia, anarthria, dysphagia, and slow eye movements. Overall, the disease was compatible with long survival. Signs of lower motor-neuron involvement were never observed, whereas motor-evoked potentials and magnetic resonance imaging demonstrated a primitive, pure degeneration of the upper motor neurons. Genotyping and linkage analyses demonstrated that this infantile-onset ascending hereditary spastic paralysis (IAHSP) is allelic to the condition previously reported as juvenile amyotrophic lateral sclerosis at the ALS2 locus on chromosome 2q33-35 (LOD score 6.66 at recombination fraction 0). We analyzed ALS2, recently found mutated in consanguineous Arabic families presenting either an ALS2 phenotype or juvenile-onset primary lateral sclerosis (JPLS), as a candidate gene. In 4 of the 10 families, we found abnormalities: three deletions and one splice-site mutation. All the mutations lead to a truncated alsin protein. In one case, the mutation affected both the short and the long alsin transcript. In the six remaining families, absence of cDNA ALS2 mutations suggests either mutations in regulatory ALS2 regions or genetic heterogeneity, as already reported in JPLS. Alsin mutations are responsible for a primitive, retrograde degeneration of the upper motor neurons of the pyramidal tracts, leading to a clinical continuum from infantile (IAHSP) to juvenile forms with (ALS2) or without (JPLS) lower motor-neuron involvement. Further analyses will determine whether other hereditary disorders with primitive involvement of the central motor pathways, as pure forms of spastic paraplegia, could be due to alsin dysfunction.

Original languageEnglish
Pages (from-to)518-527
Number of pages10
JournalAmerican Journal of Human Genetics
Volume71
Issue number3
DOIs
Publication statusPublished - Sep 2002

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Motor Neurons
Mutation
Genes
Paraplegia
Retrograde Degeneration
Efferent Pathways
Motor Evoked Potentials
Pyramidal Tracts
Quadriplegia
Genetic Heterogeneity
Nucleic Acid Regulatory Sequences
Amyotrophic Lateral Sclerosis
Deglutition Disorders
Eye Movements
Upper Extremity
Genetic Recombination
Juvenile Amyotrophic Lateral Sclerosis 2
Infantile-Onset Ascending Hereditary Spastic Paralysis
Complementary DNA
Chromosomes

ASJC Scopus subject areas

  • Genetics

Cite this

Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene. / Eymard-Pierre, Eleonore; Lesca, Gaetan; Dollet, Sandra; Santorelli, Filippo Maria; Di Capua, Matteo; Bertini, Enrico; Boespflug-Tanguy, Odile.

In: American Journal of Human Genetics, Vol. 71, No. 3, 09.2002, p. 518-527.

Research output: Contribution to journalArticle

Eymard-Pierre, Eleonore ; Lesca, Gaetan ; Dollet, Sandra ; Santorelli, Filippo Maria ; Di Capua, Matteo ; Bertini, Enrico ; Boespflug-Tanguy, Odile. / Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene. In: American Journal of Human Genetics. 2002 ; Vol. 71, No. 3. pp. 518-527.
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