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1.
Eur J Hosp Pharm ; 30(3): 180-182, 2023 05.
Artigo em Inglês | MEDLINE | ID: mdl-34103395

RESUMO

West syndrome is a severe epilepsy syndrome characterised by the appearance of drug-resistant epileptic disorders associated with hypsarrhythmia and intellectual disability. Among non-pharmacological treatments, the ketogenic diet, which consists of low carbohydrate intake and a rich lipid intake, stands out. This treatment induces a state of ketosis, which has been related to a decrease in the number of seizures. It is essential to control the carbohydrate intake within drug treatment for these patients since many pharmaceutical forms, specifically liquid oral medication, may contain carbohydrates in the form of mono/polysaccharides or polyols. We describe the case report of an infant with drug-resistant West syndrome, treated with a ketogenic diet, whose antiseizure liquid medication impeded a proper response to the diet. After the substitution of these medications, the patient showed a remarkable decrease in the number of seizures.


Assuntos
Dieta Cetogênica , Espasmos Infantis , Lactente , Humanos , Convulsões/tratamento farmacológico , Carboidratos/uso terapêutico , Preparações Farmacêuticas
2.
J Neuromuscul Dis ; 9(1): 73-82, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-34366366

RESUMO

X-linked myotubular myopathy (XLMTM) is a rare, life-threatening congenital myopathy characterized by profound skeletal muscle weakness, respiratory distress, and motor dysfunction. However, pathology is not limited to muscle and can be associated with life-threatening hepatic peliosis. Hepatobiliary disease has been reported in up to 17% of XLMTM patients but has not been extensively characterized. We report on five XLMTM patients who experienced intrahepatic cholestasis in their disease natural history, illustrating the need to further investigate these manifestations. These patients shared presentations that included pruritus, hypertransaminemia, and hyperbilirubinemia with normal gamma-glutamyl transferase, following infection or vaccination. Three patients who had genetic testing showed no evidence of genetic mutations associated with familial cholestasis. In one patient, progression to cirrhotic, decompensated liver disease occurred. Further investigations into the molecular pathomechanism underpinning these clinical observations in XLMTM patients will be important for informing patient care.


Assuntos
Colestase Intra-Hepática/etiologia , Miopatias Congênitas Estruturais/complicações , Biópsia , Evolução Fatal , Humanos , Lactente , Masculino
4.
PLoS One ; 12(1): e0170385, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28125620

RESUMO

OBJECTIVES: Analyze a set of data of hydrogen breath tests by use of data mining tools. Identify new patterns of H2 production. METHODS: Hydrogen breath tests data sets as well as k-means clustering as the data mining technique to a dataset of 2571 patients. RESULTS: Six different patterns have been extracted upon analysis of the hydrogen breath test data. We have also shown the relevance of each of the samples taken throughout the test. CONCLUSIONS: Analysis of the hydrogen breath test data sets using data mining techniques has identified new patterns of hydrogen generation upon lactose absorption. We can see the potential of application of data mining techniques to clinical data sets. These results offer promising data for future research on the relations between gut microbiota produced hydrogen and its link to clinical symptoms.


Assuntos
Testes Respiratórios/métodos , Microbioma Gastrointestinal , Intolerância à Lactose/diagnóstico , Adolescente , Criança , Pré-Escolar , Mineração de Dados , Feminino , Humanos , Lactente , Masculino
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