A novel presenilin 1 mutation resulting in familial Alzheimerʼs disease with an onset age of 29 years

WE have identified a novel Alzheimerʼs disease family in which affected subjects had a very young age of onset (range 29–35 years). Neuropathological confirmation of the diagnosis was obtained for one patient. Molecular analysis shows that within this family the disease results from a missense mutat...

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Veröffentlicht in:Neuroreport 1996-07, Vol.7 (10), p.1582-1584
Hauptverfasser: Campion, Dominique, Brice, Alexis, Dumanchin, Cecile, Puel, Michèle, Baulac, Michel, De La Sayette, Vincent, Mannequin, Didier, Duyckaerts, Charles, Michon, Agnès, Martin, Cosette, Moreau, Viviane, Penet, Christiane, Martinez, Maria, Clerget-Darpoux, Françoise, Agid, Yves, Frebourg, Thierry
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Sprache:eng
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Zusammenfassung:WE have identified a novel Alzheimerʼs disease family in which affected subjects had a very young age of onset (range 29–35 years). Neuropathological confirmation of the diagnosis was obtained for one patient. Molecular analysis shows that within this family the disease results from a missense mutation at codon 235 of the presenilin 1 (PS-1) gene. Two patients had exhibited generalized tonico-clonic seizures several years before the onset of dementia. Whether this particular clinical feature is a consequence of the PS-1 mutation remains to be established. The Leu235Pro mutation is, to our knowledge, the PS-1 mutation associated with the youngest age of AD onset, which suggests that it has a drastic effect on PS-1 function.
ISSN:0959-4965
1473-558X
DOI:10.1097/00001756-199607080-00009