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Adrenoleucodistrofia ligada al cromosoma X - Prevención

Nombres alternativos

Adrenoleucodistrofia; Adrenomieloneuropatía; Enfermedad de Addison; Adrenoleucodistrofia cerebral infantil; ALD; Complejo de Schilder-Addison

Prevención:

Se recomienda asesoría genética para los futuros padres que tienen antecedentes familiares de adrenoleucodistrofia ligada al cromosoma X. El estado portador en las mujeres se puede diagnosticar en un 85% de los casos mediante un análisis de ácidos grasos de cadena muy larga y un estudio con sonda de ADN por parte de laboratorios especializados.

El diagnóstico prenatal de la adrenoleucodistrofia ligada al cromosoma X también está disponible y se hace mediante una evaluación de células de una muestra de vellosidades coriónicas o amniocentesis.

  • Fecha de revisión: 11/12/2007
  • Versión en inglés revisada por:Rachel A. Lewis, M.D., F.A.A.P., Columbia University Pediatric Faculty Practice, New York, NY. Review provided by VeriMed Healthcare Network.
  • Traducción y localización realizada por: DrTango, Inc
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