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Congenital microcephaly in two infants with the factor V Leiden mutation.
Voudris, Konstantinos A; Skardoutsou, Angeliki; Vagiakou, Eleni A.
  • Voudris KA; Department of Neurology, P & A Kyriakou Children's Hospital, Athens, Greece. kvoudris@otenet.gr
J Child Neurol ; 17(12): 905-7, 2002 Dec.
Article en En | MEDLINE | ID: mdl-12593464
ABSTRACT
Two infants with congenital microcephaly associated with the factor V Leiden mutation are described. In both cases, brain magnetic resonance imaging (MRI) revealed cerebral atrophy and porencephalic cystic lesions, which were probably attributable to prenatal cerebral vascular events. These findings suggest that assessment for this mutation is an important part of the evaluation of infants with unexplained congenital microcephaly, especially in cases with infarcts and/or porencephalic cysts on brain MRI.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Factor V / Corteza Cerebral / Mutación Puntual / Microcefalia Límite: Female / Humans / Infant Idioma: En Año: 2002 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Factor V / Corteza Cerebral / Mutación Puntual / Microcefalia Límite: Female / Humans / Infant Idioma: En Año: 2002 Tipo del documento: Article