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Severe neurological crisis in adult patients with Tyrosinemia type 1.
Dawson, Charlotte; Ramachandran, Radha; Safdar, Samreen; Murphy, Elaine; Swayne, Orlando; Katz, Jonathan; Newsome, Philip N; Geberhiwot, Tarekegn.
Afiliação
  • Dawson C; Department of Diabetes, Endocrinology and Metabolism, Queen Elizabeth Hospital Birmingham, NHS Foundation Trust, Birmingham, United Kingdom.
  • Ramachandran R; Adult Inherited Metabolic Disease Unit, Guy's and St Thomas NHS Foundation Trust, London, United Kingdom.
  • Safdar S; Department of Diabetes, Endocrinology and Metabolism, Queen Elizabeth Hospital Birmingham, NHS Foundation Trust, Birmingham, United Kingdom.
  • Murphy E; Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom.
  • Swayne O; Neurorehabilitation Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom.
  • Katz J; Department of Endocrinology, Royal Free London NHS Foundation Trust, London, United Kingdom.
  • Newsome PN; National Institute for Health Research, Birmingham Biomedical Research Centre at University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.
  • Geberhiwot T; Centre for Liver & Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Ann Clin Transl Neurol ; 7(9): 1732-1737, 2020 09.
Article em En | MEDLINE | ID: mdl-32820610
We report six adult patients with Tyrosinaemia type 1 (HT-1) who presented with recurrent porphyria-like neurological crises after discontinuation/interruption of 2-(2-nitro-4-trifluoro-methylbenzyol)-1,3 cyclohexanedione (NTBC) treatment. The crises were life-threatening for some of the patients, with respiratory muscle paralysis requiring ventilatory support, hemodynamic disturbance due to autonomic changes requiring resuscitation, acute progressive ascending motor neuropathy causing profound impairment, recurrent seizures, and neuropathic pain. Our patients' porphyria-like presentations were variably misdiagnosed, with delay to diagnosis resulting in more severe recurrent attacks. We report the first series of neurological crises in adult patients with HT-1. These crises, which may be fatal, can be prevented and treated effectively with neurologist/physician awareness and patient education.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Respiratória / Convulsões / Doenças do Sistema Nervoso Autônomo / Doenças do Sistema Nervoso Periférico / Tirosinemias / Neuralgia Limite: Adult / Female / Humans / Male Idioma: En Revista: Ann Clin Transl Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Respiratória / Convulsões / Doenças do Sistema Nervoso Autônomo / Doenças do Sistema Nervoso Periférico / Tirosinemias / Neuralgia Limite: Adult / Female / Humans / Male Idioma: En Revista: Ann Clin Transl Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido