ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene

Background: amyotrophic lateral sclerosis (ALS) is a progressive neurological disorder. The mutations of Cu/Zn superoxide dismutase gene (SOD1) are responsible for familial ALS. We investigated a large family of Istro-Rumanian origin characterized by an autosomal dominant ALS occurring in 18 cases (three of which are still alive) throughout six generations. Methods: clinical data were available for nine patients from the 2nd generation onward, among which one contained the neuropathological. details. The mean age at onset of the disease (SD) was 57.3 +/- 8.9 years (range 49-72), while the duration of the disease spanned over a length of time equal to 4.9 +/- 1.96 years (range 1.5-7). The analysis of the coding region of SOD1 was done by PCR and direct sequencing. The SOD1 activity was measured by using the red and mononuclear cells belonging to three of the patients. Results: the leul44phe mutation of SOD1 was identified in four patients while a normal sequence was found in five healthy related subjects. The molecular defect was responsible for a decrease in SOD1 activity. Most of patients in this family presented clinical manifestations of ALS (in particular, the lower limb onset variant) not as severe as typical ALS caused by other SOD1 mutations. However, one patient suffering from hyperthyroidism for 17 years, showed an early onset and a rapidly progressing ALS coupled with dementia. Conclusions: we described a large family with a relatively not severe phenotype of ALS (due to a leul44phe SOD1 mutation) that was compromised in one patient by a concomitant hyperthyroidism. (C) 2001 Elsevier Science B.V. All rights reserved.