DAR A CONOCER LA ENFERMEDAD, CONTRIBUIR A LA INVESTIGACIÓN,
ACABAR CON LA SOLEDAD DE LOS ENFERMOS
Informaciones, actividades y boletines informativos
Información relativa a las investigaciones sobre Cutis Laxa
Acabar con la soledad de los enfermos en todo el mundo
Está en el sitio web de la asociación » Cutis Laxa Internationale «.
Nuestras páginas están dirigidas a todos los afectados por esta enfermedad genética rara, Cutis Laxa:
a enfermos y a familias de enfermos, pero también a profesionales de salud y a cualquier persona sensibilizada a las problemáticas de las enfermedades raras.
No aceptamos publicidad y no recibimos fondos de la publicidad.
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