A Case of Angelman Syndrome / 대한소아신경학회지
Journal of the Korean Child Neurology Society
;
(4): 359-364, 1999.
Artículo
en Coreano
| WPRIM
| ID: wpr-194153
ABSTRACT
Angelman syndrome is a rare genetic disorder characterized by developmental delay, speech impairment, ataxic gait, paroxysmal laughter, and seizures. The diagnosis is suspected in infants who have the characteristic clinical features and electroencephalographic (EEG) abnormalities, and is confirmed by the genetic identification of a maternally derived 15q11-13 deletion. We report a case of genetically confirmed Angelman syndrome who had the characteristic clinical and EEG features.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Convulsiones
/
Cromosomas Humanos Par 15
/
Síndrome de Angelman
/
Diagnóstico
/
Electroencefalografía
/
Marcha
/
Trastornos del Desarrollo del Lenguaje
/
Risa
Tipo de estudio:
Estudio diagnóstico
Límite:
Humanos
/
Lactante
Idioma:
Coreano
Revista:
Journal of the Korean Child Neurology Society
Año:
1999
Tipo del documento:
Artículo
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