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Dyskinetic crisis in GNAO1-related disorders: clinical perspectives and management strategies.
Domínguez Carral, Jana; Reinhard, Carola; Ebrahimi-Fakhari, Darius; Dorison, Nathalie; Galosi, Serena; Garone, Giacomo; Malenica, Masa; Ravelli, Claudia; Serdaroglu, Esra; van de Pol, Laura A; Koy, Anne; Leuzzi, Vincenzo; Roubertie, Agathe; Lin, Jean-Pierre; Doummar, Diane; Cif, Laura; Ortigoza-Escobar, Juan Darío.
Afiliação
  • Domínguez Carral J; Member of the ERN EpiCARE, Epilepsy Unit, Department of Child Neurology, Institut de Recerca Sant Joan de Déu, Barcelona, Spain.
  • Reinhard C; Centre for Rare Diseases and Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen, Tübingen, Germany.
  • Ebrahimi-Fakhari D; European Reference Network for Rare Neurological Diseases (ERN-RND), Tübingen, Germany.
  • Dorison N; Movement Disorders Program, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Galosi S; Dyspa Unit, Pediatric Neurosurgery, Hôpital Fondation Rothschild, Paris, France.
  • Garone G; Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.
  • Malenica M; Neurology, Epilepsy and Movement Disorders Unit, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Ravelli C; Department of Neuroscience, Mental Health and Sensory Organs (NESMOS), Faculty of Medicine and Psychology, Sapienza University of Rome, Rome, Italy.
  • Serdaroglu E; Member of the ERN EpiCARE, Department of Pediatrics, University Hospital Center Sestre Milosrdnice, Zagreb, Croatia.
  • van de Pol LA; Sorbonne Université, Service de Neuropédiatrie-Pathologie du développement, Centre de référence neurogénétique, Hôpital Trousseau AP-HP.SU, Paris, France.
  • Koy A; Department of Pediatric Neurology, Gazi University Faculty of Medicine, Ankara, Türkiye.
  • Leuzzi V; Emma Children's Hospital, Amsterdam Universitary Medical Centers, Amsterdam, Netherlands.
  • Roubertie A; Department of Child Neurology, Amsterdam Universitary Medical Centers, Vrije Universiteit, Amsterdam, Netherlands.
  • Lin JP; Department of Pediatrics, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
  • Doummar D; Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.
  • Cif L; CHU Montpellier, Département de Neuropédiatrie, INM, Université de Montpellier, Inserm U, Montpellier, France.
  • Ortigoza-Escobar JD; Children's Neurosciences Department, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
Front Neurol ; 15: 1403815, 2024.
Article em En | MEDLINE | ID: mdl-38903163
ABSTRACT

Background:

GNAO1-related disorders (GNAO1-RD) encompass a diverse spectrum of neurodevelopmental and movement disorders arising from variants in the GNAO1 gene. Dyskinetic crises, marked by sudden and intense exacerbations of abnormal involuntary movements, present a significant challenge in GNAO1-RD.

Objectives:

This study aimed to establish a standardized framework for understanding dyskinetic crises, addressing crucial aspects such as definition, triggers, diagnostic criteria, complications, and management strategies.

Methods:

A Delphi consensus process was conducted involving international experts in GNAO1-RD. The panel of thirteen experts participated in three voting rounds, discussing 90 statements generated through a literature review and clinical expertise.

Results:

Consensus was achieved on 31 statements, defining dyskinetic crises as abrupt, paroxysmal episodes involving distinct abnormal movements in multiple body regions, triggered by emotional stress or infections. Dyskinetic crises may lead to functional impairment and complications, emphasizing the need for prompt recognition. While individualized pharmacological recommendations were not provided, benzodiazepines and clonidine were suggested for acute crisis management. Chronic treatment options included tetrabenazine, benzodiazepines, gabapentin, and clonidine. Deep brain stimulation should be considered early in the treatment of refractory or prolonged dyskinetic crisis.

Conclusion:

This consensus provides a foundation for understanding and managing dyskinetic crises in GNAO1-RD for clinicians, caregivers, and researchers. The study emphasizes the importance of targeted parental and caregiver education, which enables early recognition and intervention, thereby potentially minimizing both short- and long-term complications. Future research should concentrate on differentiating dyskinetic crises from other neurological events and investigating potential risk factors that influence their occurrence and nature. The proposed standardized framework improves clinical management, stakeholder communication, and future GNAO1-RD research.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article