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How to differentiate frontotemporal from Alzheimer's dementia? Recent developments in molecular genetics and neuropathology = Kako ločiti fronto-temporalno od Alzheimerjeve demence? Najnovejša odkritja molekularne genetike in nevropatologijeLiščić, RajkaFrontotemporal dementia is a major cause of non-Alzheimer dementia (AD). Frontotemporallobar degeneration (FTLD) is used here as an umbrella term for both clinical and neuropathological entities ... starting before age of 65 years. FTLD differs clinically from ADbecause memory loss is rarely an early symptom.Instead, the dementia of FTLD is usually denoted by behavioral and language difficulties, although clinical and cognitive features of FTLD may overlap with AD. Aphasia may be prominent, either fluent or nonfluent. Clinical FTLD is associated with a variety of different neuropathological entities, which share common feature of preferential degeneration of the frontal and temporal lobes. Whereas, in the past, most attention focused on FTLD pathology associated with tau-positive inclusions and microtubule associated protein tau gene (MAPT) mutations (tauopathies), there has recentlybeen greater attention paid to non-tau, ubiquitin positive inclusions (FTLD-U) or non-tauopathies. It is now recognized that FTLD-U is the most common pathology associated with clinical FTLD. Clinically, cases with FTLD-U may additionally present with or without motor neuron disease and parkinsonism. Majority of familial cases of FTLD-U have mutations in the progranulin (PRGN) gene. Some families of FTLD-U with PGRN mutation (hereditary dysphasic disinhibition dementia 1 and 2) are characterized, besides behavior and language difficulties, by additional memory loss and AD-type pathology. Recently, the ubiquitinated pathological protein in FTLD-U has been identified as TAR DNA binding protein (TDP 43) and found in an increasing number of neurodegenerative diseases, including AD. The overlap between FTLD-U and AD is important since as many as 20 % of AD cases show someFTLD-U type TDP-43 pathology. Recent developments have helped to clarify the relationship between different types of FTLD and related conditions. (Abstract truncated at 2000 characters)Vir: Zdravniški vestnik : glasilo Slovenskega zdravniškega društva = Slovenian medical journal = journal of Slovenian Medical Association. - ISSN 1318-0347 (Letn. 77, supl. II, maj 2008, str. II-71-II-74)Vrsta gradiva - članek, sestavni delLeto - 2008Jezik - angleškiCOBISS.SI-ID - 24290009
Avtor
Liščić, Rajka
Teme
Dementia |
Diagnosis |
Genetics |
Alzheimer's Disease |
Phenotype |
DNA-Binding Proteins |
Diagnosis, Differential |
Fenotip |
Demenca |
DNA-vezalne beljakovine |
Diagnostika diferencialna |
nevrologija |
Alzheimerjeva bolezen |
fronto-temporalna degeneracija |
molekularna genetika |
diagnostika
vir: Zdravniški vestnik : glasilo Slovenskega zdravniškega društva = Slovenian medical journal = journal of Slovenian Medical Association. - ISSN 1318-0347 (Letn. 77, supl. II, maj 2008, str. II-71-II-74)
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