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Fetal Pediatr Pathol ; 32(4): 308-11, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23301919

RESUMO

Neuroimaging and molecular cytogenetics were used to ascertain the cause of disability in a case. The case was diagnosed to be a variant of Miller-Dieker syndrome (MDS). Retrospective analysis showed a prenatal scan reporting dolichocephaly. We evaluated dolichocephaly, the name associated with a nonsynostotic cause to be a physiological variant having no prognostic value, to that of a similar synostotic or secondary to a neurological disorder cause, with prognostic significance. The report confirmed early craniosynostosis in cases suspected with a neurological disorder and also on an important criterion in molecular testing strategy in cases suspected with MDS.


Assuntos
Lissencefalias Clássicas e Heterotopias Subcorticais em Banda/diagnóstico , Cabeça/anormalidades , Ultrassonografia Pré-Natal , Pesos e Medidas Corporais , Feminino , Humanos , Gravidez
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