Cerebral white matter abnormalities in 6p25 deletion syndrome.
AJNR Am J Neuroradiol
; 27(3): 586-8, 2006 Mar.
Article
en En
| MEDLINE
| ID: mdl-16551997
ABSTRACT
Submicroscopic deletion of the terminal part of the short arm of chromosome 6, including 6p25, leads to developmental retardation, hearing impairment, ocular dysgenesis, and dysmorphic features. We diagnosed 3 patients referred because of white matter abnormalities of unknown origin. MR imaging showed multifocal areas of abnormal signal and enlarged perivascular spaces in the cerebral white matter that were stable during follow-up. Multifocal white matter abnormalities are most commonly seen in static, nonmetabolic encephalopathies, including chromosomal abnormalities.
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Anomalías Múltiples
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Cromosomas Humanos Par 6
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Encéfalo
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Imagen por Resonancia Magnética
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Discapacidades del Desarrollo
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Anomalías del Ojo
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Deleción Cromosómica
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Anomalías Craneofaciales
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Pérdida Auditiva
Límite:
Child
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Child, preschool
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Female
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Humans
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Male
Idioma:
En
Año:
2006
Tipo del documento:
Article