Lymphodysplasia and kras mutation: a case report and literature review.

We describe the clinical data of one case of CFC syndrome, genetically determined by KRAS mutation, that involved chylothorax, lymphedema, sinus pericranii, craniosynostosis, and seizures. This is the second case report of the literature.
PMID: 26939159 [PubMed - in process]

Source: Lymphology - March 6, 2016 Category: Internal Medicine Tags: Lymphology Source Type: research