Test Prenatal Molecular

El screening prenatal molecular permite analizar el genoma del futuro recién nacido de una forma mucho más detallada y en menos tiempo mediante una nueva herramienta llamada chip de ADN o microarray.Los chips de ADN permiten detectar pérdidas y ganancias submicroscópicas

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de material genético. El array de prenatal analiza alrededor de 150 regiones del genoma causantes de enfermedades genéticas que comportan trastornos graves del desarrollo (retraso


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mental, autismo, malformaciones congénitas,…) y que, a pesar de su pequeño tamaño, son detectables mediante esta técnica. Los arrays permiten detectar hasta un 32% más de anomalías que la citogenética convencional.


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