Perlman syndrome

Perlman syndrome is characterized principally by polyhydramnios, neonatal macrosomia, bilateral renal tumors (hamartomas with or without nephroblastomatosis), hypertrophy of the islets of Langerhans and facial dysmorphism.

Also known as: Perlman syndrome, nephroblastomatosis - foetal ascites - macrosomia - Wilms tumour, nephroblastomatosis, foetal ascites, macrosomia and Wilms tumour, nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome, nephroblastomatosis-fetal ascites-macrosomia-Wilms tumour syndrome, renal hamartomas, nephroblastomatosis and fetal gigantism, renal hamartomas, nephroblastomatosis and foetal gigantism, PRLMNS

0 clinical trials for this condition and its sub-types, 0 tagged with Perlman syndrome itself.