Literature DB >> 28247171

Genetic Counseling Dilemmas for a Patient with Sporadic Amyotrophic Lateral Sclerosis, Frontotemporal Degeneration & Parkinson's Disease.

Vittorio Mantero1, Claudia Tarlarini2, Angelo Aliprandi3, Giuseppe Lauria4, Andrea Rigamonti3, Lucia Abate5, Paola Origone6, Paola Mandich7, Silvana Penco2, Andrea Salmaggi3.   

Abstract

Amyotrophic lateral sclerosis (ALS), frontotemporal degeneration and Parkinson's disease may be different expressions of the same neurodegenerative disease. However, association between ALS and parkinsonism-dementia complex (ALS-PDC) has only rarely been reported apart from the cluster detected in Guam. We report a patient presenting with ALS-PDC in whom pathological mutations/expansions were investigated. No other family members were reported to have any symptoms of a neurological condition. Our case demonstrates that ALS-PDC can occur as a sporadic disorder, even though the coexistence of the three clinical features in one patient suggests a single underlying genetic cause. It is known that genetic testing should be preferentially offered to patients with ALS who have affected first or second-degree relatives. However, this case illustrates the importance of genetic counseling for family members of patients with sporadic ALC-PDC in order to provide education on the low recurrence risk. Here, we dicuss the ethical, psychological and practical consequences for patients and their relatives.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; Dementia; Frontotemporal degeneration; Genetic; Genetic counseling; Genetic test; Guam complex; Parkinson disease; Parkinsonism

Mesh:

Year:  2017        PMID: 28247171     DOI: 10.1007/s10897-017-0088-5

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  24 in total

Review 1.  El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis.

Authors:  B R Brooks; R G Miller; M Swash; T L Munsat
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2000-12

2.  Parkinsonism-dementia complex, an endemic disease on the island of Guam. I. Clinical features.

Authors:  A HIRANO; L T KURLAND; R S KROOTH; S LESSELL
Journal:  Brain       Date:  1961-12       Impact factor: 13.501

3.  Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.

Authors:  Mariely DeJesus-Hernandez; Ian R Mackenzie; Bradley F Boeve; Adam L Boxer; Matt Baker; Nicola J Rutherford; Alexandra M Nicholson; NiCole A Finch; Heather Flynn; Jennifer Adamson; Naomi Kouri; Aleksandra Wojtas; Pheth Sengdy; Ging-Yuek R Hsiung; Anna Karydas; William W Seeley; Keith A Josephs; Giovanni Coppola; Daniel H Geschwind; Zbigniew K Wszolek; Howard Feldman; David S Knopman; Ronald C Petersen; Bruce L Miller; Dennis W Dickson; Kevin B Boylan; Neill R Graff-Radford; Rosa Rademakers
Journal:  Neuron       Date:  2011-09-21       Impact factor: 17.173

Review 4.  Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.

Authors:  M Sabatelli; A Conte; M Zollino
Journal:  Clin Genet       Date:  2013-03-12       Impact factor: 4.438

5.  Familial amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii Peninsula of Japan: clinical and neuropathological study and tau analysis.

Authors:  S Kuzuhara; Y Kokubo; R Sasaki; Y Narita; T Yabana; M Hasegawa; T Iwatsubo
Journal:  Ann Neurol       Date:  2001-04       Impact factor: 10.422

6.  Coexistence of parkinsonism, dementia and upper motor neuron syndrome in four Czech patients.

Authors:  Katerina Farníková; Petr Kanovský; Igor Nestrasil; Pavel Otruba
Journal:  J Neurol Sci       Date:  2010-09-15       Impact factor: 3.181

7.  A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.

Authors:  J B Leverenz; C E Yu; T J Montine; E Steinbart; L M Bekris; C Zabetian; L K Kwong; V M-Y Lee; G D Schellenberg; T D Bird
Journal:  Brain       Date:  2007-04-17       Impact factor: 13.501

8.  Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population.

Authors:  Lucia Corrado; Stefania Battistini; Silvana Penco; Laura Bergamaschi; Lucia Testa; Claudia Ricci; Fabio Giannini; Giuseppe Greco; Maria Cristina Patrosso; Simona Pileggi; Renzo Causarano; Letizia Mazzini; Patricia Momigliano-Richiardi; Sandra D'Alfonso
Journal:  J Neurol Sci       Date:  2007-04-25       Impact factor: 3.181

9.  Amyotrophic lateral sclerosis with dementia showing clinical parkinsonism and severe degeneration of the substantia nigra: report of an autopsy case.

Authors:  Masayuki Shintaku; Kiyomitsu Oyanagi; Daita Kaneda
Journal:  Neuropathology       Date:  2007-06       Impact factor: 1.906

10.  Biochemical and ultrastructural study of neurofibrillary tangles in amyotrophic lateral sclerosis/parkinsonism-dementia complex in the Kii peninsula of Japan.

Authors:  Nobuo Itoh; Koichi Ishiguro; Hiroyuki Arai; Yasumasa Kokubo; Ryogen Sasaki; Yugo Narita; Shigeki Kuzuhara
Journal:  J Neuropathol Exp Neurol       Date:  2003-07       Impact factor: 3.685

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  1 in total

Review 1.  Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review.

Authors:  Ashley Crook; Chris Jacobs; Toby Newton-John; Rosie O'Shea; Alison McEwen
Journal:  J Neurol       Date:  2021-03-01       Impact factor: 6.682

  1 in total

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