RT Journal Article
SR Electronic
T1 A patient with loss of vision in the right eye and neurofibromatosis type 1
JF Canadian Medical Association Journal
JO CMAJ
FD Canadian Medical Association
SP 203
OP 206
DO 10.1503/cmaj.080706
VO 180
IS 2
A1 Mumoli, Nicola
A1 Cei, Marco
A1 Bartolomei, Carlo
A1 Pirillo, Vania
YR 2009
UL http://www.cmaj.ca/content/180/2/203.abstract
AB Abstract: Neurofibromatosis type 1 is a common autosomal dominant condition that affects about 1 in 5000 people. We describe a 75-year-old man who, in addition to many classic developmental changes of the disease in his skin, eyes and nervous system, had blindness in his right eye as a complication.