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Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatment.
Dufournet, B; Nguyen, K; Charles, P; Grabli, D; Jacquette, A; Borg, M; Danaila, T; Mutez, E; Drapier, S; Colin, O; Eusebio, A; Philip, N; Azulay, J P.
Affiliation
  • Dufournet B; Department of Clinical Neurosciences (Movement Disorders), Timone University Hospital (AP-HM), 264 rue Saint Pierre, 13385 Marseille Cedex 5, France; Aix-Marseille University, Marseille, France. Electronic address: boris.dufournet@ap-hm.fr.
  • Nguyen K; Department of Genetics (Neurogenetics), Timone University Hospital (AP-HM), Marseille, France; Aix-Marseille University, Marseille, France.
  • Charles P; Department of Genetics (Neurogenetics), Pitié-Salpêtrière University Hospital (AP-HP), Paris, France; Sorbonne University, UPMC Paris 06 (UMR S 1127, CNRS UMR 7225, ICM), Paris, France.
  • Grabli D; Department of Neurology (Movement Disorders), Pitié-Salpêtrière University Hospital (AP-HP), Paris, France; Sorbonne University, UPMC Paris 06 (UMR S 1127, CNRS UMR 7225, ICM), Paris, France.
  • Jacquette A; Department of Genetics (Neurogenetics), Pitié-Salpêtrière University Hospital (AP-HP), Paris, France; Sorbonne University, UPMC Paris 06 (UMR S 1127, CNRS UMR 7225, ICM), Paris, France.
  • Borg M; Department of Clinical Neurosciences (Movement Disorders), Nice University Hospital, Nice, France.
  • Danaila T; Department of Neurology (Movement Disorders), Pierre Wertheimer University Hospital (HCL), Lyon, France; Lyon-1 University, Marc Jeannerod Center for Cognitives Neurosciences (CNRS UMR 5229), Lyon, France.
  • Mutez E; Department of Neurosciences (Movement Disorders), Lille University Hospital, Lille, France; Lille University (INSERM U1171), Lille, France.
  • Drapier S; Department of Neurology (Movement Disorders), Rennes University Hospital, Rennes, France; Rennes-1 University (URU 4712 "Basal Ganglia & Behavior"), Rennes, France.
  • Colin O; Department of Neurology (Movement Disorders), Poitiers University Hospital, Poitiers, France; Clinical Investigation Center (INSERM CIC 0802 & INSERM U1084, Clinical and Experimental Neurosciences), Poitiers University Hospital, Poitiers, France.
  • Eusebio A; Department of Clinical Neurosciences (Movement Disorders), Timone University Hospital (AP-HM), 264 rue Saint Pierre, 13385 Marseille Cedex 5, France; Aix-Marseille University, Marseille, France.
  • Philip N; Department of Genetics (Neurogenetics), Timone University Hospital (AP-HM), Marseille, France; Aix-Marseille University, Marseille, France.
  • Azulay JP; Department of Clinical Neurosciences (Movement Disorders), Timone University Hospital (AP-HM), 264 rue Saint Pierre, 13385 Marseille Cedex 5, France; Aix-Marseille University, Marseille, France.
Rev Neurol (Paris) ; 173(6): 406-410, 2017 Jun.
Article in En | MEDLINE | ID: mdl-28461026
BACKGROUND: While it is known that 22q11.2 microdeletions (22q11.2-del) increase the risk of Parkinson's disease (PD), the characteristics of PD associated with 22q11.2-del have not been specifically explored. OBJECTIVE: This report aimed to assess the clinical characteristics and treatment responses of PD patients with 22q11.2-del, and to describe any features that might lead neurologists to investigate the comorbidity. METHODS: Nine PD patients (eight men, one woman) with 22q11.2-del were followed at seven centers of the French PD Expert Network (Ns-Park). RESULTS: PD diagnosis was made before 22q11.2-del diagnosis in seven cases; their main characteristics were early onset (32-48 years) and good initial levodopa sensitivity, but with a course characterized by severe and early-onset levodopa-induced motor complications and psychiatric manifestations. Three patients received deep brain stimulation (DBS) that was effective. CONCLUSION: Searching for 22q11.2-del in PD patients presenting with suggestive features is relevant as the clinical presentation is similar to idiopathic PD, but with other associated characteristics, including a severe evolution. Results with DBS are similar to those reported for idiopathic PD.
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Full text: 1 Database: MEDLINE Main subject: Parkinson Disease / 22q11 Deletion Syndrome Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Rev Neurol (Paris) Year: 2017 Type: Article

Full text: 1 Database: MEDLINE Main subject: Parkinson Disease / 22q11 Deletion Syndrome Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Rev Neurol (Paris) Year: 2017 Type: Article