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1.
Ugeskr Laeger ; 169(23): 2216-9, 2007 Jun 04.
Artigo em Dinamarquês | MEDLINE | ID: mdl-17592690

RESUMO

INTRODUCTION: Critically-ill patients in intensive care units often suffer from weakness of the arms and legs and have difficulty in weaning from the ventilator. If this cannot be explained by the illness itself, it may be due to a critical illness polyneuropathy (CIP) or a critical illness myopathy (CIM) or both. It is difficult to determine the cause of the weakness by conventional methods in an intensive care unit. The objective was to describe the diagnostic yield with electrodiagnostic testing and describe the various patterns and prognosis in these patients. MATERIALS AND METHODS: 55 consecutive patients with a critical illness associated with unexplained weakness of limbs and often respiratory muscles were studied to estimate motor and sensory nerve conduction, electromyography, direct muscle stimulation, and repetitive nerve stimulation. RESULTS: 18 patients had CIM, 16 had CIP and in 9 a combination of CIM and CIP was found. Direct muscle stimulation was more sensitive to show myogenic affection than needle EMG in this patient group. CONCLUSION: Electrophysiologic tests are valuable in identifying the specific cause of prolonged weakness in critically-ill patients in intensive care units.


Assuntos
Estado Terminal , Doenças Neuromusculares/diagnóstico , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Debilidade Muscular/diagnóstico , Debilidade Muscular/etiologia , Doenças Musculares/diagnóstico , Doenças Musculares/etiologia , Doenças Musculares/fisiopatologia , Doenças Neuromusculares/etiologia , Doenças Neuromusculares/fisiopatologia , Polineuropatias/diagnóstico , Polineuropatias/etiologia , Polineuropatias/fisiopatologia , Fatores de Risco
2.
Ugeskr Laeger ; 167(35): 3310-1, 2005 Aug 29.
Artigo em Dinamarquês | MEDLINE | ID: mdl-16138977

RESUMO

Kennedy's disease, or spinal and bulbar muscular atrophy (SBMA), is an inherited X-linked degenerative disorder characterised by slowly progressive proximal limb weakness, bulbar weakness, fasciculations, signs of androgen insensitivity and characteristic EMG findings. The disease is caused by a trinucleotide (CAG) repeat in the androgen receptor gene. We describe a patient with atypical symptoms who was initially misdiagnosed after presenting with weakness of mm. masseter and mm. temporales that caused his jaw to hang open. The initial diagnosis was suspicion of myasthenia gravis or ALS. Genetic testing later confirmed the diagnosis of Kennedy's disease.


Assuntos
Arcada Osseodentária , Atrofia Muscular Espinal/diagnóstico , Diagnóstico Diferencial , Eletromiografia , Humanos , Arcada Osseodentária/fisiopatologia , Masculino , Músculo Masseter/fisiopatologia , Pessoa de Meia-Idade , Debilidade Muscular/diagnóstico , Debilidade Muscular/fisiopatologia , Atrofia Muscular Espinal/genética , Atrofia Muscular Espinal/fisiopatologia
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