Neurofibromatosis type 2

Neurofibromatosis type 2 (NF2) is a tumor-prone disorder characterized by the development of multiple schwannomas and meningiomas.

Retinal hamartoma

A hamartoma (a benign, focal malformation consisting of a disorganized mixture of cells and tissues) of the retina.


Total: 1

                      


(per page)
PMID (PMCID)
19629903
MALE Infant, Newborn
Infantile onset neurofibromatosis type 2 presenting with peripheral facial palsy, skin patches, retinal hamartoma and foot drop.
Tibussek D, Hubsch S, Berger K, Schaper J, Rosenbaum T, Mayatepek E.
Klin Padiatr. 2009;221(4):247-50.
Infantile onset neurofibromatosis type 2 presenting with peripheral facial palsy, skin patches, retinal hamartoma and foot drop.