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Entrevista en @copepinares para hablar sobre el #sindromenoonan y nuestra asociación
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Creciendo Con Noonan
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Este es el único exoesqueleto pediátrico del mundo destinado a niños que padecen Atrofia Muscular Espinal, una enfermedad rara y degenerativa #Futura



DYK that an estimated 1 in 1,000 to 1 in 2,500 births worldwide are diagnosed with #NoonanSyndrome? Genetic testing for NS can confirm a diagnosis, impact care, and affect medical decisions for patients and their families. #NoonSyndromeAwarenessDay ow.ly/oBqk50I1L8B















Excited to announce our next webinar: 👉Oct. 24, 4 pm ET Learn about behavior in the #RASopathies bit.ly/2Y5L8rQ