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1.
Neurosurg Rev ; 38(4): 603-18, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25732522

RESUMO

In the first weeks following aneurysmal subarachnoid haemorrhage, cerebrovascular alterations may impact the outcome significantly. Diagnosis of cerebral vasospasm and detection of alterations at risk of delayed cerebral ischemia are key targets to be monitored in the post-acute phase. Available tools include clinical monitoring, as well as studies that can detect possible arterial narrowing, alterations of perfusion, metabolism and neurophysiology. Each technique is able to investigate possible vascular impairment and has different advantages and limits. All available techniques have been described. Among these, the most practical have been selected and compared for their peculiar characteristics. Based on this analysis, a flowchart to monitor these patients is finally proposed.


Assuntos
Isquemia Encefálica/etiologia , Hemorragia Subaracnóidea/complicações , Hemorragia Subaracnóidea/diagnóstico , Vasoespasmo Intracraniano/complicações , Vasoespasmo Intracraniano/diagnóstico , Isquemia Encefálica/epidemiologia , Humanos , Risco
2.
Am J Med Genet A ; 132A(2): 202-5, 2005 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-15578573

RESUMO

We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, skull defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.


Assuntos
Anormalidades Múltiplas/patologia , Encéfalo/anormalidades , Displasia Ectodérmica/patologia , Linfangiectasia Intestinal/patologia , Crânio/anormalidades , Anormalidades Múltiplas/genética , Feminino , Humanos , Lactente , Cariotipagem , Proteína Reelina , Síndrome
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