Genetic Counseling for Frontotemporal Dementias

被引:0
|
作者
Kimberly A. Quaid
机构
[1] Indiana University School of Medicine,Department of Medical and Molecular Genetics
来源
关键词
Frontotemporal dementia; Genetic counseling;
D O I
暂无
中图分类号
学科分类号
摘要
Frontotemporal dementia (FTD) is an umbrella term for a heterogeneous group of neurodegenerative disorders that are characterized by changes in cognition, language, personality, and social functioning. Approximately 40% of individuals with FTD have a family history of dementia, but less than 10% have a clear autosomal dominant pattern of inheritance. However, establishing a clear mode of inheritance in FTD is complicated by clinical heterogeneity, variable expression, phenocopies, misdiagnosis, early death due to other causes, missing medical records, and lost family histories. Mutations in the microtubule-associated protein tau and progranulin genes have been reported in the majority of hereditary cases, making genetic testing of at-risk individuals possible. The first step in counseling a family with a history of FTD is to take a comprehensive family history with confirmation of any diagnosis in a family member with medical records to the extent possible. If the pedigree analysis suggests an autosomal dominant pattern of inheritance, genetic testing of an affected relative may be offered to the family to determine if a mutation is present. If a mutation is found, relatives interested in pursuing genetic testing should be referred to a genetic counselor familiar with genetic testing for neurodegenerative disorders. Predictive testing of unaffected and at-risk relatives should only be offered in the context of a comprehensive genetic counseling protocol offering pre- and post-test counseling and support. One survey of at-risk individuals in a large family with FTD found that 50% were interested in testing. In one study actually offering genetic testing for FTD, the rate of uptake of testing was only 8.4%. A more recent study estimated the uptake for testing for FTD to be somewhere between 7% and 17% and attributed the low uptake to family resistance to testing. While genetic testing may be appropriate for some families with Alzheimer's disease and FTD, uptake of testing may be expected to be low.
引用
收藏
页码:706 / 709
页数:3
相关论文
共 50 条
  • [41] New Approaches to Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Degeneration
    Goldman, Jill S.
    [J]. CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2012, 12 (05) : 502 - 510
  • [42] A Decade of Genetic Counseling in Frontotemporal Dementia Affected Families: Few Counseling Requests and much Familial Opposition to Testing
    Riedijk, S. R.
    Niermeijer, M. F. N.
    Dooijes, D.
    Tibben, A.
    [J]. JOURNAL OF GENETIC COUNSELING, 2009, 18 (04) : 350 - 356
  • [43] In vivo cholinergic circuit evaluation in frontotemporal and Alzheimer dementias
    Di Lazzaro, V
    Pilato, F
    Dileone, M
    Saturno, E
    Oliviero, A
    Marra, C
    Daniele, A
    Ranieri, F
    Gainotti, G
    Tonali, PA
    [J]. NEUROLOGY, 2006, 66 (07) : 1111 - 1113
  • [44] Hippocampal sclerosis dementia - Expanding the phenotypes of frontotemporal dementias?
    Lippa, CF
    Dickson, DW
    [J]. NEUROLOGY, 2004, 63 (03) : 414 - 415
  • [45] Biochemical and molecular characterization of neurofibrillary degeneration in frontotemporal dementias
    Delacourte, A
    [J]. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 1999, 10 : 75 - 79
  • [46] TDP-43 Proteinopathies: ALS and Frontotemporal Dementias
    Prudlo, J.
    [J]. FORTSCHRITTE DER NEUROLOGIE PSYCHIATRIE, 2009, 77 : S25 - S27
  • [47] Cellular, molecular and biochemical neuropathology of frontotemporal dementias (FTD)
    Trojanowski, JQ
    [J]. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2004, 17 (04) : 376 - 376
  • [48] Frontotemporal dementias: main syndromes and underlying brain changes
    Piguet, Olivier
    Kumfor, Fiona
    [J]. CURRENT OPINION IN NEUROLOGY, 2020, 33 (02) : 215 - 221
  • [49] Cerebellar structural connectivity and contributions to cognition in frontotemporal dementias
    Chen, Yu
    Landin-Romero, Ramon
    Kumfor, Fiona
    Irish, Muireann
    Hodges, John R.
    Piguet, Olivier
    [J]. CORTEX, 2020, 129 : 57 - 67
  • [50] Defining the spectrum of frontotemporal dementias associated with TARDBP mutations
    Caroppo, Paola
    Camuzat, Agnes
    Guillot-Noel, Lena
    Thomas-Anterion, Catherine
    Couratier, Philippe
    Wong, Tsz Hang
    Teichmann, Marc
    Golfier, Veronique
    Auriacombe, Sophie
    Belliard, Serge
    Laurent, Bernard
    Lattante, Serena
    Millecamps, Stephanie
    Clot, Fabienne
    Dubois, Bruno
    van Swieten, John C.
    Brice, Alexis
    Le Ber, Isabelle
    [J]. NEUROLOGY-GENETICS, 2016, 2 (03)