RESUMEN
The syndrome of malignant migrating partial seizures of infancy (MMPSI) is characterized by early onset of multiple seizure types and overall poor prognosis. Seizures are markedly drug resistant and few reports have suggested the efficacy of some antiepileptic drugs. We report one case of MMPSI in which prolonged seizure control is obtained with an association of clonazepam, levetiracetam and stiripentol, confirming thus the possibility of complete sustained seizure control in this epileptic syndrome. Of more than 60 cases reported to date, ours is the forth in which sustained complete control of seizures was obtained.
Asunto(s)
Anticonvulsivantes/uso terapéutico , Clonazepam/uso terapéutico , Dioxolanos/uso terapéutico , Epilepsias Parciales/tratamiento farmacológico , Convulsiones/tratamiento farmacológico , Electroencefalografía , Femenino , Movimientos de la Cabeza , Humanos , Lactante , Imagen por Resonancia Magnética , Vómitos/etiologíaRESUMEN
OBJECTIVE: To test the hypothesis that predisposition to childhood herpes simplex virus (HSV) type 1 encephalitis (HSE) may be determined in part by human genetic factors. STUDY DESIGN: A genetic epidemiologic survey of childhood HSE (onset at age 3 months to 15 years) over a 20-year period (1985-2004) was conducted throughout France (comprising 29 university hospital neuropediatric centers). A total of 85 children fulfilled the diagnostic criteria for inclusion. Family and personal histories were obtained by face-to-face interview for 51 patients. RESULTS: No familial cases of HSE were identified in our survey; however, a high proportion (20%) of the children interviewed had a relevant family history: parental consanguinity (12% of patients), early-onset herpetic keratitis in a first-degree relative (6%), or both (2%). The narrow window of high susceptibility to HSE before age 3 years (62% of patients) further indicates that predisposition to HSE is tightly age-dependent. CONCLUSIONS: This survey suggests that childhood HSE, although sporadic, may result from Mendelian predisposition (from autosomal recessive susceptibility in particular), at least in some children. There likely is incomplete penetrance, however, which may reflect, at least in part, the impact of age at the time of HSV-1 infection.
Asunto(s)
Encefalitis por Herpes Simple/genética , Encefalitis por Herpes Simple/virología , Variación Genética , Receptor Toll-Like 3/genética , Aciclovir/uso terapéutico , Adolescente , Factores de Edad , Edad de Inicio , Antivirales/uso terapéutico , Niño , Preescolar , Encefalitis por Herpes Simple/tratamiento farmacológico , Femenino , Predisposición Genética a la Enfermedad , Variación Genética/genética , Humanos , Lactante , Masculino , Factores de Riesgo , Simplexvirus , Adulto JovenRESUMEN
Herpes simplex virus-1 (HSV-1) encephalitis (HSE) is the most common form of sporadic viral encephalitis in western countries. Its pathogenesis remains unclear, as it affects otherwise healthy patients and only a small minority of HSV-1-infected individuals. Here, we elucidate a genetic etiology for HSE in two children with autosomal recessive deficiency in the intracellular protein UNC-93B, resulting in impaired cellular interferon-alpha/beta and -lambda antiviral responses. HSE can result from a single-gene immunodeficiency that does not compromise immunity to most pathogens, unlike most known primary immunodeficiencies. Other severe infectious diseases may also reflect monogenic disorders of immunity.
