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Trisomies 13 and 18. You are here:  . Via Cal del Poz, 26. 31010 Farra di Soligo (TV). Is a ‘Support Oganizaton For Trisomy’. Founded by parents for parents of Trisomy children, SOFT Italia is a voluntary association providing support for families of children born with Patau’s Syndrome (Trisomy 13), Edward’s Syndrome (Trisomy 18) and related chromosomal disorders. Puts families in contact with one another and offers support during prenatal diagnosis, during the life of the child and after.

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Trisomies 13 and 18. You are here:  . Via Cal del Poz, 26. 31010 Farra di Soligo (TV). Is a ‘Support Oganizaton For Trisomy’. Founded by parents for parents of Trisomy children, SOFT Italia is a voluntary association providing support for families of children born with Patau’s Syndrome (Trisomy 13), Edward’s Syndrome (Trisomy 18) and related chromosomal disorders. Puts families in contact with one another and offers support during prenatal diagnosis, during the life of the child and after.

LINKS TO THIS WEBSITE

internationaltrisomyalliance.com internationaltrisomyalliance.com

ITA Advisors - International Trisomy 13/18 Alliance

http://www.internationaltrisomyalliance.com/ita-advisors.html

International Trisomy 13/18 Alliance. TRIS Project: Ongoing research. International Trisomy Alliance Advisors. International Trisomy Alliance is in the process of inviting professionals who are involved in research and the care and support of those affected by trisomy 13 and 18 to join our Professional Advisors, and parents involved in groups or organizations providing support to families to join our Parent Advisors. John C. Carey. MD, MP.H. MD, Ph.D. Deborah A. Bruns. Annette Hollingsworth - Moore.

internationaltrisomyalliance.com internationaltrisomyalliance.com

Trisomy Support Groups for Trisomy 13 and Trisomy 18 - International Trisomy 13/18 Alliance

http://www.internationaltrisomyalliance.com/trisomy-support-groups.html

International Trisomy 13/18 Alliance. TRIS Project: Ongoing research. Hover over the links below for information, and click the link to visit the website, or email if there is no website. Please note, however, that we have no control over the nature, content or availability of those sites. 26085;本 Japan. 26085;本 Japan. Families often use social networks like Facebook to ask questions and share with other parents. Please use the contact form. Face Book Support Groups. Leve med trisomi 13 og trisomi 18.

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Home

Trisomies 13 and 18. You are here:  . Via Cal del Poz, 26. 31010 Farra di Soligo (TV). Is a ‘Support Oganizaton For Trisomy’. Founded by parents for parents of Trisomy children, SOFT Italia is a voluntary association providing support for families of children born with Patau’s Syndrome (Trisomy 13), Edward’s Syndrome (Trisomy 18) and related chromosomal disorders. Puts families in contact with one another and offers support during prenatal diagnosis, during the life of the child and after.

trisomia.prv.pl trisomia.prv.pl

Zespół Downa

Zespół Downa, choroba genetyczna 21 chromosomu, edukacja dzieci niepełnosprawnych intelektualnie. Zespół downa, dawid góral,rewalidacja, rehabilitacja. Strona znajduje się pod adresem www.from.okay.pl/goral/downstrona/index.html.

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Trisomía 18, Información y apoyo a familias con niños con síndrome de Edwards

PORQUE ESTÁN VIVOS Y LO PODEMOS HACER MEJOR. Los niños con trisomía 18 están vivos y hay diversas acciones que pueden ayudar a darles una mejor calidad de vida, independientemente del tiempo que estén con nosotros. Buscamos entregar la mayor información posible, tal que las familias puedan optar a las mejores decisiones para su hija o hijo, idealmente en conjunto con su médico. Iquest;QUÉ SON LAS TRISOMÍAS? Iquest;QUÉ ES LA TRISOMÍA 18 Y LA TRISOMÍA 13? En general cada óvulo y cada espermatozoide ...

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Asociación Trisomía 13, Trisomía 18 y. Otras malformaciones genéticas graves. Tu embarazo y parto. Esta es una página impulsada por familias que residen en España y que, en algún momento, experimentaron un diagnóstico de trisomía 18 (síndrome de Edwards) o trisomía 13 (síndrome de Patau) para uno de sus hijos. Para ellos ofrecemos nuestras vivencias y nuestra esperanza.

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Sindrome de Down

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Trisomía 21

No es casualidad que el día de hoy… TÚ estés aquí. La gracia de tener una persona en nuestra familia con Trisomia 21, es la fortuna de tener cerca a un maestr@ que nos enseñará el verdadero sentido de ser humano. Ahora eres más especial que nunca. Papá y Mamá se han convertido en unos padres extraordinarios y muy especiales. 150 % más felices. Crees que ellos van a sufrir en la vida…? Ellos serán más felices que muchos de nosotros. Bienvenido a compartir el mundo desde otra perspectiva.