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Enfermedad de Moya-Moya y gestación
P.A. Doblas, M.A. Barber, I. Eguiluz, E. Valdivia, J.R. Andérica, I. Aguilera, M. Suárez, S. Luna, M. Abehsera
Departamento de Ginecología y Obstetricia. Hospital Materno-Infantil. Complejo Regional Hospitalario Carlos-Haya. Málaga. España.
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        "titulo" => "Summary"
        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Moya-Moya disease is a rare occlusive entity&#44; progressive with time and of scarce prevalence or global distribution&#46; It is due to stenosis of the intracraneal portion of the internal carotid artery&#44; with establishment of compensatory secondary intracraneal anastamoses at different levels &#40;leptomeningeal&#44; basal ganglion&#44; and transdurals&#41;&#46; There is a higher incidence during the first five years of life &#40;juvenile form&#41; or in the third decade &#40;adult form&#41;&#46; Its course is cerebral hypoperfusion&#44; which in clinical terms translates into recurrent intracraneal haemorrhages and transient ischaemic attacks&#46; With reference to our speciality&#44; an elevated risk of complications during pregnancy has been described&#44; with caesarean section being recommended before term&#46;</p>"
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  ]
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  "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0210573X02771530?idApp=UINPBA00004N"
]
Información del artículo
ISSN: 0210573X
Idioma original: Español
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