Les décisions relatives à la planification familiale peuvent être difficiles et susciter beaucoup d’émotions lorsque l’un des parents potentiels est atteint d’une maladie génétique, comme le syndrome de Marfan. Avant toute décision, les parents doivent connaître les nombreuses options actuellement disponibles ainsi que les risques encourus par l’enfant et la mère. Un conseiller en génétique ou l’infirmier du Centre d’aide et de ressources de la Fondation Marfan peut aborder ces options avec vous et vous fournir des informations.
Related Resources
Loeys-Dietz Syndrome
Loeys-Dietz syndrome is a genetic disorder of connective tissue. Because connective tissue is found throughout the body, Loeys-Dietz syndrome features can occur in the heart, blood vessels, bones, joints, skin, and internal organs, such as the intestines, spleen, and uterus. Some Loeys-Dietz syndrome features are easy to see. Others features, such as heart and blood […]
Genetic Testing and Marfan Syndrome
Genetic testing for mutations in fibrillin-1 (FBN1) and other genes has become an important and reliable option to aid in the diagnosis of Marfan syndrome and related disorders. However, the results of genetic testing for the diagnosis of disorders are not always straightforward. Therefore, working with a medical geneticist (a physician with training in genetics) […]
Tags: Marfan Syndrome , Patients & Families
Know the signs.
Fight for victory.
Join us in the fight for victory over Marfan syndrome and related conditions and help us create a brighter future for everyone living with these conditions.