摘要
Background: Cases of early-onset Alzheimer disease (AD)with an autosomal dominant inheritance pattern (familial AD FAD ) are rare but have greatly advanced our understanding of the molecular pathogenesis of AD. We describe herein a kindred with very early-onset FAD (age, < 40 years) with unusual pathological features and a novel mutation in the presenilin 1 (PSEN1) gene (S170F) and review the existing literature on very early-onset FAD. Objective: To analyze the neuropathological and genetic features of a family with onset of AD in the third decade of life. Design, Setting, and Participants: The proband underwent full clinical assessment and postmortem examination at the Washington University Alzheimer’s Disease Research Center, St Louis, Mo. Limited pathological samples and autopsy records of 2 affected family members were available. The proband underwent screening for mutations in genes linked with FAD. Results: Dementia developed in 3 family members in this kindred at a mean age of 27 years; the proband had myoclonus, seizures, and rigidity, similar to findings in previously described kindreds with PSEN1 mutations. All 3 family members were confirmed to have AD by neuropathological examination. The proband also had widespread Lewy body pathology in the brainstem, limbic areas, and neocortex; specific staining for Lewy bodies was not performed in the other 2 family members. The proband had a single mutation (S170F)in exon 6 of the PSEN1 gene, which segregates with disease. Conclusions: A novel PSEN1 mutation causes very early-onset FAD with associated Lewy bodies. To our knowledge, this kindred has the earliest reported onset of pathologically confirmed FAD and dementia with Lewy bodies.
Background： Cases of early-onset Alzheimer disease （AD） with an autosomal dominant inheritance pattern （familial AD [ FAD ] ） are rare but have greatly advanced our understanding of the molecular pathogenesis of AD. We describe herein a kindred with very early-onset FAD （age, 〈 40 years） with unusual pathological features and a novel mutation in the presenilin 1 （PSEN1） gene （S170F） and review the existing literature on very early-onset FAD. Objective： To analyze the neuropathological and genetic features of a family with onset of AD in the third decade of life. Design, Setting, and Participants： The proband underwent full clinical assessment and postmortem examination at the Washington University Alzheimer＇s Disease Research Center, St Louis, Mo. Limited pathological samples and autopsy records of 2 affected family members were available. The proband underwent screening for mutations in genes linked with FAD. Results： Dementia developed in 3 family members in this kindred at a mean age of 27 years; the proband had myoclonus, seizures, and rigidity, similar to findings in previously described kindreds with PSEN1 mutations. All 3 family members were confirmed to have AD by neuropathological examination. The proband also had widespread Lewy body pathology in the brainstem, limbic areas, and neocortex; specific staining for Lewy bodies was not performed in the other 2 family members. The proband had a single mutation （S170F）in exon 6 of the PSEN1 gene, which segregates with disease. Conclusions： A novel PSEN1 mutation causes very early-onset FAD with associated Lewy bodies. To our knowledge, this kindred has the earliest reported onset of pathologically confirmed FAD and dementia with Lewy bodies.
出处
《世界核心医学期刊文摘（神经病学分册）》
2006年第6期5-5,共1页
Digest of the World Core Medical Journals:Clinical Neurology
