Original Research Article
Familial Frontotemporal Dementia Associated with a Novel Presenilin-1 MutationTang-Wai D.a · Lewis P.e,f · Boeve B.a,f · Hutton M.e,f · Golde T.e,f · Baker M.e,f · Hardy J.e,f · Michels V.b · Ivnik R.c,f · Jack C.d,f · Petersen R.a,f
Departments of aNeurology, bMedical Genetics, cPsychiatry and Psychology and dDiagnostic Radiology, Mayo Clinic, Rochester, Minn., eDepartment of Science and Neurogenetics Laboratory, Mayo Clinic, Jacksonville, Fla., fMayo Alzheimer’s Disease Research Center, Mayo Clinic and Mayo Foundation, Rochester, Minn., USA
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We report a kindred with three cases of dementia. The proband presented with forgetfulness and personality changes at age 56, followed shortly thereafter by behavioral dyscontrol, hyperphagia, hypersexuality, delusions, illusions, disinhibition and double incontinence. Neuroimaging studies were consistent with frontotemporal dementia (FTD). In one allele, an arginine insertion at codon 352 in the presenilin 1 (PSEN1) gene was identified; no mutation was identified in the amyloid precursor protein or tau genes. We conclude that the clinical features of the Kluver-Bucy syndrome and FTD can be associated with PSEN1 mutations. Furthermore, presenilin analyses may be helpful to characterize kindreds with familial dementing illnesses regardless of the phenotype, particularly if no tau mutation is present.
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