Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
1.
Eur J Paediatr Neurol ; 6(3): 143-52, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12363101

RESUMEN

The authors report eight children, who presented in the first year of life with isolated head stereotypies, that corresponded neither to the usual normal 'rhythmic habit patterns of infancy', nor to various types of abnormal repetitive head movements described in young children. Their head stereotypies closely resembled those described in bobble-head doll syndrome. The neurological status evidenced axial hypotonia, ataxia, oculomotor abnormalities, motor and language delay. The patients were followed for several years clinically and with video recordings. No single aetiology was found. Computed tomography (CT) or magnetic resonance imaging (MRI) show a congenital cerebellar abnormality in two children but no hydrocephalus. The outcome of these children showed in all but one patient a normal cognitive and psychosocial development, even though the head stereotypies are still present in six of eight patients and all remain significantly clumsy. The association of head stereotypies and motor delay should prompt a search for cerebellar congenital malformation. The outcome of those patients was much better than originally anticipated and these head stereotypies are not related either to mental retardation, or to psychopathology. The possible mechanisms involved are also discussed.


Asunto(s)
Ataxia Cerebelosa/patología , Discapacidades del Desarrollo/patología , Trastorno de Movimiento Estereotipado/patología , Adolescente , Adulto , Encéfalo/patología , Ataxia Cerebelosa/fisiopatología , Cerebelo/anomalías , Niño , Preescolar , Diagnóstico Diferencial , Femenino , Estudios de Seguimiento , Cabeza , Humanos , Lactante , Recién Nacido , Imagen por Resonancia Magnética , Masculino , Examen Neurológico , Trastornos de la Motilidad Ocular/patología , Trastorno de Movimiento Estereotipado/fisiopatología , Factores de Tiempo , Tomografía Computarizada por Rayos X
2.
J Affect Disord ; 115(1-2): 177-82, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-18790541

RESUMEN

BACKGROUND: A large body of evidence suggests that immune system dysregulation is associated with Major Depressive Disorder (MDD) in adults. This study extends this work to adolescent MDD to examine the hypotheses of immune system dysregulation in adolescents with MDD, as manifested by significantly: (i) elevated plasma levels of cytokines (interferon [IFN]-gamma, tumor necrosis factor-alpha, interleukin [IL]-6, IL-1beta, and IL-4); and (ii) Th1/Th2 cytokine imbalance shifted toward Th1 as indexed by increased IFN-gamma/IL-4. METHOD: Thirty adolescents with MDD (19 females; 13 medication-free/naïve; ages 12-19) of at least 6 weeks duration and a minimum severity score of 40 on the Children's Depression Rating Scale-Revised, and 15 healthy comparisons (8 females), group-matched for age, were enrolled. Plasma cytokines were examined using enzyme-linked immunosorbent assay. Mann-Whitney test was used to compare subjects with MDD and controls. RESULTS: Adolescents with MDD had significantly elevated plasma IFN-gamma levels (3.38+/-11.8 pg/ml versus 0.37+/-0.64 pg/ml; p<0.003), and IFN-gamma/IL-4 ratio (16.6+/-56.5 versus 1.76+/-2.28; p=0.007). A trend for IL-6 to be elevated in the MDD group was also observed (1.52+/-2.88 pg/ml versus 0.49+/-0.90 pg/ml; p=0.09). Importantly, findings remained evident when medicated subjects were excluded. CONCLUSIONS: Findings suggest that immune system dysregulation may be associated with adolescent MDD, with an imbalance of Th1/Th2 shifted toward Th1, as documented in adult MDD. Larger studies with medication-free adolescents should follow.


Asunto(s)
Citocinas/sangre , Trastorno Depresivo Mayor/inmunología , Células TH1/inmunología , Células Th2/inmunología , Adolescente , Niño , Ensayo de Inmunoadsorción Enzimática , Femenino , Humanos , Masculino , Valores de Referencia , Adulto Joven
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA