syndrome de Marfan néonatal
A rare severe and life-threatening genetic disease occurring during the neonatal period. The disease has characteristics of classical Marfan syndrome manifestations in addition to facial dysmorphism (megalocornea, iridodonesis, ectopia lentis, crumpl
SNOMEDCT-BE (disorder) / 763839005
SNOMEDCT-BE (megalocornea, iridodonesis, ectopia lentis, crumpl / 763839005