LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 2 of total 2

Search options

  1. Article ; Online: Intrafamilial and interfamilial heterogeneity of PINK1-associated Parkinson's disease in Sudan.

    Bakhit, Yousuf / Ibrahim, Mohamed O / Tesson, Christelle / Elhassan, Ali A / Ahmed, Mohamed Anwer / Alebeed, Mohamed A / Elrasheed, Salma M / Omar, Mawia A / Abubaker, Rayan / Eltom, Khalid / Shaheen, Mutaz T / Ibrahim, Yousuf A / Almak, Murad E / Ali, Hiba A / Abugrain, Ahmed A / Almahal, Mohamed A / MohamedSharif, Abubaker A / Tahir, Mohamed Y / Malik, Sawazen M /
    Eldirdiri Abdelrahman, Hazim / Khidir, Reem J / Mohamed, Malaz T / Abdalla, Abdelmohaymin / Elsayed, Liena E O / Lesage, Suzanne / Corvol, Jean-Christophe / Seidi, Osheik / Wüllner, Ullrich

    Parkinsonism & related disorders

    2023  Volume 111, Page(s) 105401

    Abstract: PINK1 is the second most predominant gene associated with autosomal recessive Parkinson's disease. Homozygous mutations in this gene are associated with an early onset of symptoms. Bradykinesia, tremors, and rigidity are common features, while dystonia, ... ...

    Abstract PINK1 is the second most predominant gene associated with autosomal recessive Parkinson's disease. Homozygous mutations in this gene are associated with an early onset of symptoms. Bradykinesia, tremors, and rigidity are common features, while dystonia, motor fluctuation, and non-motor symptoms occur in a lower percentage of cases and usually respond well to levodopa. We investigated 14 individuals with parkinsonism and eleven symptom-free siblings from three consanguineous Sudanese families, two of them multigenerational, using a custom gene panel screening 34 genes, 27 risk variants, and 8 candidate genes associated with parkinsonism. We found a known pathogenic nonsense PINK1 variant (NM_032409.3:c.1366C>T; p.(Gln456*)), a novel pathogenic single base duplication (NM_032409.3:c.1597dup; p.(Gln533Profs*29)), and another novel pathogenic insertion (NM_032409.3:c.1448_1449ins[1429_1443; TTGAG]; p.(Arg483Serfs*7)). All variants were homozygous and co-segregated in all affected family members. We also identified intrafamilial and interfamilial phenotypic heterogeneity associated with PINK1 mutations in these Sudanese cases, possibly reflecting the nature of the Sudanese population that has a large effective population size, which suggests a higher possibility of novel findings in monogenic and polygenic diseases in Sudan.
    MeSH term(s) Humans ; Parkinson Disease/genetics ; Sudan ; Parkinsonian Disorders/genetics ; Homozygote ; Mutation/genetics ; Protein Kinases/genetics ; Age of Onset
    Chemical Substances Protein Kinases (EC 2.7.-)
    Language English
    Publishing date 2023-04-25
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1311489-x
    ISSN 1873-5126 ; 1353-8020
    ISSN (online) 1873-5126
    ISSN 1353-8020
    DOI 10.1016/j.parkreldis.2023.105401
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Methylation of alpha-synuclein in a Sudanese cohort.

    Bakhit, Yousuf / Schmitt, Ina / Hamed, Ahlam / Ibrahim, Etedal Ahmed A / Mohamed, Inaam N / El-Sadig, Sarah M / Elseed, Maha A / Alebeed, Mohamed A / Shaheen, Mutaz T / Ibrahim, Mohamed O / Elhassan, Ali A / Eltom, Khalid / Ali, Hiba A / Ibrahim, Yousuf A / Almak, Murad E / Abubaker, Rayan / Ahmed, Mohamed Anwer / Abugrain, Ahmed A / Elrasheed, Salma M /
    Omar, Mawia A / Almahal, Mohamed A / MohamedSharif, Abubaker A / Tahir, Mohamed Y / Malik, Sawazen M / Eldirdiri, Hazim S / Khidir, Reem J / Mohamed, Malaz T / Abdalla, Abdelmohaymin / Omer, Farouk Yassen / Elsayed, Liena E O / Babikir, Haydar El Hadi / Bukhari, Elfateh Abd-Allah / Seidi, Osheik / Wüllner, Ullrich

    Parkinsonism & related disorders

    2022  Volume 101, Page(s) 6–8

    Abstract: Background: Several studies suggested a significant role of epigenetic changes, including alterations in miRNA, histone modifications, and DNA methylation of α-synuclein (SNCA) in Parkinson's disease (PD) pathogenicity. As of yet, only very few studies ... ...

    Abstract Background: Several studies suggested a significant role of epigenetic changes, including alterations in miRNA, histone modifications, and DNA methylation of α-synuclein (SNCA) in Parkinson's disease (PD) pathogenicity. As of yet, only very few studies have been carried out in this field in Africa and none in Sudan.
    Materials and methods: We collected DNA from 172 Sudanese individuals (90 cases, 82 controls) who donated saliva for DNA extraction (mean age of onset: 40.6 ± 22.4 years). A family history of PD was evident in 64 patients. DNA preparation and bisulfite sequencing of SNCA
    Results: Of the fourteen analyzed CpGs of SNCA
    Conclusion: We identified the presence of a specific pattern of DNA methylation in a young Sudanese cohort of familial PD, which confirms the importance of the methylation of SNCA
    MeSH term(s) Adolescent ; Adult ; DNA ; DNA Methylation/genetics ; Epigenesis, Genetic ; Humans ; Middle Aged ; Parkinson Disease/genetics ; Young Adult ; alpha-Synuclein/genetics ; alpha-Synuclein/metabolism
    Chemical Substances SNCA protein, human ; alpha-Synuclein ; DNA (9007-49-2)
    Language English
    Publishing date 2022-06-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 1311489-x
    ISSN 1873-5126 ; 1353-8020
    ISSN (online) 1873-5126
    ISSN 1353-8020
    DOI 10.1016/j.parkreldis.2022.05.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top