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Síndrome de Aarskog - Información general

Definición:

Es una enfermedad hereditaria que afecta la estatura, músculos, esqueleto, genitales y apariencia facial de una persona. Hereditaria significa que se transmite de padres a hijos.

Causas, incidencia y factores de riesgo:

El síndrome de Aarskog es un trastorno genético que afecta principalmente a los hombres, aunque las mujeres pueden tener una forma más leve. La afección es causada por cambios (mutaciones) en un gen llamado "displasia faciogenital" (FGDY1).

  • Fecha de revisión: 2/5/2008
  • Versión en inglés revisada por:Chad Haldeman-Englert, MD, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA. Review provided by VeriMed Healthcare Network.
  • Traducción y localización realizada por: DrTango, Inc
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