A Case of Ring Chromosome 20 with Mental Retardation and Epilepsy / 소아과
Korean Journal of Pediatrics
; : 108-111, 2005.
Article
en Ko
| WPRIM
| ID: wpr-42877
Biblioteca responsable:
WPRO
ABSTRACT
Ring chromosome 20 mosaicism [r(20)] is a rare chromosomal anomaly associated with minor dysmorphism, mental retardation, autistic behavior, and intractable epilepsy. The proposed mechanism of ring formation is breakage of both short and long arms of a chromosome with subsequent end-to- end fusion. We encountered an 18-month-old boy who presented with developmental delay and mental retardation with seizure episodes, but showed normal brain magnetic resonance imaging. Chromosome study from peripheral blood showed 46,XY, r(20)(p13q13.3) karyotype. The authors report a case of ring chromosome 20 with mental retardation and epilepsy, with a review of the literature.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Brazo
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Cromosomas en Anillo
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Convulsiones
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Encéfalo
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Imagen por Resonancia Magnética
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Epilepsia
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Cariotipo
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Discapacidad Intelectual
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Mosaicismo
Límite:
Humans
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Infant
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Male
Idioma:
Ko
Revista:
Korean Journal of Pediatrics
Año:
2005
Tipo del documento:
Article