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1.
J Headache Pain ; 10(5): 361-5, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19649688

RESUMO

Migraine is a common disorder in childhood and adolescence. Studies on adults show the effectiveness and tolerability of riboflavin in migraine prevention, while data on children are scarce. This retrospective study reports on our experience of using riboflavin for migraine prophylaxis in 41 pediatric and adolescent patients, who received 200 or 400 mg/day single oral dose of riboflavin for 3, 4 or 6 months. Attack frequency and intensity decreased (P < 0.01) during treatment, and these results were confirmed during the follow-up. A large number of patients (77.1%) reported that abortive drugs were effective for controlling ictal events. During the follow-up, 68.4% of cases had a 50% or greater reduction in frequency of attacks and 21.0% in intensity. Two patients had vomiting and increased appetite, respectively, most likely for causes unrelated to the use of riboflavin. In conclusion, riboflavin seems to be a well-tolerated, effective, and low-cost prophylactic treatment in children and adolescents suffering from migraine.


Assuntos
Transtornos de Enxaqueca/prevenção & controle , Riboflavina/uso terapêutico , Complexo Vitamínico B/uso terapêutico , Adolescente , Criança , Feminino , Humanos , Masculino
2.
J Child Neurol ; 24(6): 772-4, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19189931

RESUMO

Methyl-CpG-binding protein 2 (MECP2) gene mutations have been identified in girls with Rett syndrome and in boys with heterogeneous neuropsychiatric disorders. Because of the limited or inconsistent data reported in literature, the role of methyl-CpG-binding protein 2 gene in the pathogenesis of mental retardation and pervasive developmental disorders needs further study. We scanned methyl-CpG-binding protein 2 gene in 99 Italian patients with pervasive developmental disorder or with nonsyndromal mental retardation. Four methyl-CpG-binding protein 2 gene mutations were found: 2 in 4 girls with Rett disorder, the others in 2 girls with mental retardation. The wide phenotypic spectrum and the variants of methyl-CpG-binding protein 2 gene, which may play an important role in gene regulation and neurodevelopment, justify the literature's interest particularly in girls.


Assuntos
Transtornos Globais do Desenvolvimento Infantil/genética , Deficiência Intelectual/genética , Proteína 2 de Ligação a Metil-CpG/genética , Mutação , Adolescente , Criança , Análise Mutacional de DNA , Feminino , Humanos , Itália , Masculino , Fenótipo , Síndrome de Rett/genética
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