Neuropsychiatric and cognitive features in autosomal‐recessive early parkinsonism due to PINK1 mutations
Identifieur interne : 002D20 ( Main/Exploration ); précédent : 002D19; suivant : 002D21Neuropsychiatric and cognitive features in autosomal‐recessive early parkinsonism due to PINK1 mutations
Auteurs : Lilach Ephraty [Israël] ; Omer Porat [Israël] ; David Israeli [Israël] ; Oren S. Cohen [Israël] ; Olga Tunkel [Israël] ; Shinar Yael [Israël] ; Yasaku Hatano [Japon] ; Nobutaka Hattori [Japon] ; Sharon Hassin-Baer [Israël]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-03-15.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Adult, Cognition Disorders (complications), Cognition Disorders (diagnosis), Consanguinity, Early Diagnosis, Female, Humans, Male, Mental Disorders (complications), Mental Disorders (diagnosis), Mental Disorders (psychology), Mutation, Nervous system diseases, Neuropsychiatry, Neuropsychological Tests, PINK1, Parkinsonian Disorders (complications), Parkinsonian Disorders (genetics), Parkinsonism, Pedigree, Point Mutation (genetics), Protein Kinases (genetics), Severity of Illness Index, cognitive, hereditary, neuropsychiatry.
- MESH :
- chemical , genetics : Protein Kinases.
- complications : Cognition Disorders, Mental Disorders, Parkinsonian Disorders.
- diagnosis : Cognition Disorders, Mental Disorders.
- genetics : Parkinsonian Disorders, Point Mutation.
- psychology : Mental Disorders.
- Adult, Consanguinity, Early Diagnosis, Female, Humans, Male, Neuropsychological Tests, Pedigree, Severity of Illness Index.
Abstract
Autosomal‐recessive early‐onset Parkinsonism (AREP) due to PINK1 mutations is characterized by an early‐onset, slowly progressive disease, with a good response to levodopa. Psychiatric and cognitive disturbances associated with AREP have rarely been reported in the literature. We describe 2 brothers from a Jewish–Iraqi consanguineous family with a homozygous PINK1 nonsense mutation. Both patients presented with anxiety and dysphoria accompanied by a gait disturbance that developed subsequently into a clinical depression. During the course of the disease, both developed drug‐induced behavioral disturbances of the hedonistic homeostatic dysregulation type and 1 had drug‐induced psychosis. The first patient had been diagnosed with mild mental retardation and during the 22 years of disease had further deteriorated; the second developed frontal‐type dementia at an early age, 20 years after onset. Their father had a psychiatric disorder but no Parkinsonism. This report expands the phenotypic profile of PINK1‐related disease, presenting unique psychiatric and cognitive features as part of the clinical picture. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21319
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Autosomal‐recessive early‐onset Parkinsonism (AREP) due to PINK1 mutations is characterized by an early‐onset, slowly progressive disease, with a good response to levodopa. Psychiatric and cognitive disturbances associated with AREP have rarely been reported in the literature. We describe 2 brothers from a Jewish–Iraqi consanguineous family with a homozygous PINK1 nonsense mutation. Both patients presented with anxiety and dysphoria accompanied by a gait disturbance that developed subsequently into a clinical depression. During the course of the disease, both developed drug‐induced behavioral disturbances of the hedonistic homeostatic dysregulation type and 1 had drug‐induced psychosis. The first patient had been diagnosed with mild mental retardation and during the 22 years of disease had further deteriorated; the second developed frontal‐type dementia at an early age, 20 years after onset. Their father had a psychiatric disorder but no Parkinsonism. This report expands the phenotypic profile of PINK1‐related disease, presenting unique psychiatric and cognitive features as part of the clinical picture. © 2007 Movement Disorder Society</div>
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