Matches in SemOpenAlex for { <https://semopenalex.org/work/W2767687660> ?p ?o ?g. }
- W2767687660 endingPage "1523" @default.
- W2767687660 startingPage "1504" @default.
- W2767687660 abstract "Clinical-pathological studies remain the gold-standard for the diagnosis of Parkinson's disease (PD). However, mounting data from genetic PD autopsies challenge the diagnosis of PD based on Lewy body pathology. Most of the confirmed genetic risks for PD show heterogenous neuropathology, even within kindreds, which may or may not include Lewy body pathology. We review the literature of genetic PD autopsies from cases with molecularly confirmed PD or parkinsonism and summarize main findings on SNCA (n = 25), Parkin (n = 20, 17 bi-allelic and 3 heterozygotes), PINK1 (n = 5, 1 bi-allelic and 4 heterozygotes), DJ-1 (n = 1), LRRK2 (n = 55), GBA (n = 10 Gaucher disease patients with parkinsonism), DNAJC13, GCH1, ATP13A2, PLA2G6 (n = 8 patients, 2 with PD), MPAN (n = 2), FBXO7, RAB39B, and ATXN2 (SCA2), as well as on 22q deletion syndrome (n = 3). Findings from autopsies of heterozygous mutation carriers of genes that are traditionally considered recessively inherited are also discussed. Lewy bodies may be present in syndromes clinically distinctive from PD (eg, MPAN-related neurodegeneration) and absent in patients with clinical PD syndrome (eg, LRRK2-PD or Parkin-PD). Therefore, the authors can conclude that the presence of Lewy bodies are not specific to the diagnosis of PD and that PD can be diagnosed even in the absence of Lewy body pathology. Interventions that reduce alpha-synuclein load may be more justified in SNCA-PD or GBA-PD than in other genetic forms of PD. The number of reported genetic PD autopsies remains small, and there are limited genotype-clinical-pathological-phenotype studies. Therefore, larger series of autopsies from genetic PD patients are required. © 2017 International Parkinson and Movement Disorder Society." @default.
- W2767687660 created "2017-11-17" @default.
- W2767687660 creator A5037098776 @default.
- W2767687660 creator A5082051712 @default.
- W2767687660 date "2017-11-01" @default.
- W2767687660 modified "2023-10-12" @default.
- W2767687660 title "Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature" @default.
- W2767687660 cites W1252660048 @default.
- W2767687660 cites W1497114979 @default.
- W2767687660 cites W1513071869 @default.
- W2767687660 cites W1527671059 @default.
- W2767687660 cites W1553794588 @default.
- W2767687660 cites W1929625487 @default.
- W2767687660 cites W1964353444 @default.
- W2767687660 cites W1965398181 @default.
- W2767687660 cites W1965641455 @default.
- W2767687660 cites W1965778124 @default.
- W2767687660 cites W1966327969 @default.
- W2767687660 cites W1967823816 @default.
- W2767687660 cites W1968746015 @default.
- W2767687660 cites W1969611978 @default.
- W2767687660 cites W1972097907 @default.
- W2767687660 cites W1972943699 @default.
- W2767687660 cites W1973738022 @default.
- W2767687660 cites W1976870579 @default.
- W2767687660 cites W1977044612 @default.
- W2767687660 cites W1979460584 @default.
- W2767687660 cites W1979486721 @default.
- W2767687660 cites W1979527613 @default.
- W2767687660 cites W1980449640 @default.
- W2767687660 cites W1981515077 @default.
- W2767687660 cites W1983044117 @default.
- W2767687660 cites W1987572257 @default.
- W2767687660 cites W1988056635 @default.
- W2767687660 cites W1988457275 @default.
- W2767687660 cites W1988979381 @default.
- W2767687660 cites W1991925532 @default.
- W2767687660 cites W1992632425 @default.
- W2767687660 cites W1993136260 @default.
- W2767687660 cites W1999810443 @default.
- W2767687660 cites W2000193504 @default.
- W2767687660 cites W2001307857 @default.
- W2767687660 cites W2002269285 @default.
- W2767687660 cites W2004194290 @default.
- W2767687660 cites W2004865303 @default.
- W2767687660 cites W2004918356 @default.
- W2767687660 cites W2005920762 @default.
- W2767687660 cites W2007348345 @default.
- W2767687660 cites W2008234948 @default.
- W2767687660 cites W2008827081 @default.
- W2767687660 cites W2009270310 @default.
- W2767687660 cites W2010331279 @default.
- W2767687660 cites W2011339216 @default.
- W2767687660 cites W2011977459 @default.
- W2767687660 cites W2015533185 @default.
- W2767687660 cites W2017345592 @default.
- W2767687660 cites W2019895460 @default.
- W2767687660 cites W2020427460 @default.
- W2767687660 cites W2021097923 @default.
- W2767687660 cites W2021209363 @default.
- W2767687660 cites W2022289010 @default.
- W2767687660 cites W2023009129 @default.
- W2767687660 cites W2023506905 @default.
- W2767687660 cites W2025374131 @default.
- W2767687660 cites W2026148937 @default.
- W2767687660 cites W2028650990 @default.
- W2767687660 cites W2030857589 @default.
- W2767687660 cites W2030916925 @default.
- W2767687660 cites W2031921753 @default.
- W2767687660 cites W2032481706 @default.
- W2767687660 cites W2040140774 @default.
- W2767687660 cites W2043792709 @default.
- W2767687660 cites W2044843068 @default.
- W2767687660 cites W2047087015 @default.
- W2767687660 cites W2048982523 @default.
- W2767687660 cites W2050310121 @default.
- W2767687660 cites W2050453654 @default.
- W2767687660 cites W2051087311 @default.
- W2767687660 cites W2051157328 @default.
- W2767687660 cites W2051753710 @default.
- W2767687660 cites W2052742260 @default.
- W2767687660 cites W2053160507 @default.
- W2767687660 cites W2053606072 @default.
- W2767687660 cites W2054811240 @default.
- W2767687660 cites W2056363797 @default.
- W2767687660 cites W2057668962 @default.
- W2767687660 cites W2058857521 @default.
- W2767687660 cites W2058900917 @default.
- W2767687660 cites W2060122517 @default.
- W2767687660 cites W2061621819 @default.
- W2767687660 cites W2063037378 @default.
- W2767687660 cites W2063127941 @default.
- W2767687660 cites W2063690790 @default.
- W2767687660 cites W2065808064 @default.
- W2767687660 cites W2068160127 @default.
- W2767687660 cites W2070199486 @default.
- W2767687660 cites W2070435517 @default.
- W2767687660 cites W2071419252 @default.