RiskGYNE

Visión general

RiskGYNE es nuestra prueba BRCA más completa que verifica las mutaciones de los genes BRCA1 y BRCA2 relacionadas con el cáncer de mama y ovario hereditario, así como de otros 22 genes relacionados también con estos dos tipos de cáncer y también con el cáncer uterino.

 

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Fundamentos del test RiskGYNE

RiskGYNE captura y secuencia las regiones genómicas de 24 genes, utilizando técnicas modernas de Next Generation Sequencing (NGS) en combinación con enfoques más clásicos de genética molecular.

En este sentido, con RiskGYNE es posible detectar mutaciones puntuales en exones, regiones intrónicas profundas (hasta 45bb) y en regiones reguladoras no traducidas de los genes, así como algunas variantes estructurales.

La lista completa de los genes que RiskGYNE analiza es:

  • ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MRE11A, MSH2, MSH6, MUTYH, NBN, NF1, PALB2, PMS2, POLD1, PTEN, RAD50, RAD51C, RAD51D, STK11 y TP53.

Indicaciones de uso de RiskGYNE

RiskGYNE está indicado para detectar mutaciones de los genes BRCA1 y BRCA2, así como otras de otros 22 genes relacionadas estrechamente con el cáncer de mama, cáncer de ovario y cáncer uterino hereditario, situándose, nuestro test RiskGYNE, como el más completo del mercado en pacientes con riesgo de cáncer ginecológico hereditario.

Además, a diferencia de otros tests de BIOPROGNOS para ayuda en el diagnóstico (como los tests OncoBREAST Dx, OncoLUNG Dx, OncoOVARIAN Dx, OncoPROSTATE Dx o OncoCUP Dx), RiskGYNE no necesita prescripción médica.

Cómo hacerse el test RiskGYNE

Una vez completado el proceso de compra a través de esta página web, recibirá un Saliva Kit para tomar una muestra de su saliva en su domicilio o la dirección indicada.

 

 

Una vez que reciba nuestro Saliva Kit, simplemente siga las instrucciones incluidas y devuelva la caja proporcionada con franqueo pagado.

Transcurridos unos 20 días hábiles (según su ubicación), los resultados de su test RiskGYNE se le enviarán por correo electrónico a la dirección proporcionada durante el proceso de compra.

Referencias

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  2. Kuchenbaecker KB, Hopper JL, Barnes DR, et al. Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers. JAMA 2017; 317(23):2402-2416.
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