Co-occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2.

Ramón PecesRocío MenaYolanda MartínConcepción HernándezCarlos PecesDolores TelleríaEmilio CuestaRafael SelgasPablo LapunzinaJulián Nevado

Published in: Molecular genetics & genomic medicine (2020)

Despite the presence of both conditions there was not additive effect of NF1 and PKD2 in terms of the severity of tumor development and/or ADPKD progression.

Keyphrases

polycystic kidney disease
optic nerve
optical coherence tomography
signaling pathway
high grade
lps induced
oxidative stress
pi k akt
nuclear factor
immune response