El síndrome de Noonan es un trastorno genético que provoca defectos cardíacos, problemas de hemorragia, rasgos faciales distintivos, etc. El médico le explica qué signos debe buscar en un bebé y en un niño.
Esta enfermedad genética no tiene cura. Sin embargo, hay muchos tratamientos que, trabajando conjuntamente, pueden aliviar los síntomas y evitar problemas más graves.
La pérdida de audición es difícil de detectar en los bebés. El médico le explicará cómo se evalúa la audición de los recién nacidos y qué hacer si su bebé puede tener una pérdida auditiva.
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