Cerebral white matter abnormalities in 6p25 deletion syndrome.
AJNR Am J Neuroradiol
; 27(3): 586-8, 2006 Mar.
Article
em 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
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Anormalidades Múltiplas
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Cromossomos Humanos Par 6
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Encéfalo
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Imageamento por Ressonância Magnética
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Deficiências do Desenvolvimento
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Anormalidades do Olho
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Deleção Cromossômica
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Anormalidades Craniofaciais
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Perda Auditiva
Limite:
Child
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Child, preschool
/
Female
/
Humans
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Male
Idioma:
En
Revista:
AJNR Am J Neuroradiol
Ano de publicação:
2006
Tipo de documento:
Article
País de afiliação:
Holanda