HOMOCISTINURIA GENETICA PDF

Skip to search form Skip to main content You are currently offline. Some features of the site may not work correctly. La hemocistinuria es una enfermedad genetica caracterizada por la deficiencia de diversas enzimas vinculadas al metabolismo de la metionina. La presencia de eventos tromboticos y tromboembolicos constituye la principal causa de mortalidad y morbilidad en estos pacientes. Se describen 2 hermanos de 5 y 9 anos,que presentaron episodios compatibles con accidente cerebrovascular.

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Todos los paneles siguientes son inmediatamente disponibles para hacer pruebas en Breda Genetics. Hallazgos incidentales : a pedido. Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website.

These cookies do not store any personal information. Saltar al contenido Todos los paneles siguientes son inmediatamente disponibles para hacer pruebas en Breda Genetics.

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Todos los paneles siguientes son inmediatamente disponibles para hacer pruebas en Breda Genetics. Hallazgos incidentales : a pedido. Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information. Saltar al contenido Todos los paneles siguientes son inmediatamente disponibles para hacer pruebas en Breda Genetics.

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Homocistinuria y accidente cerebrovascular en la infancia

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