Neurofibromatosis Type 1 with Subacute Sclerosing Panencephalitis: A Rare Coexistence
Neurofibromatosis type 1 is an autosomal dominant disorder with variable expressivity. The major diagnostic features are cafe-au-lait spots, neurofibromas, Lisch nodules of the iris, optic glioma, axillary freckling and bony dysplasia. Affected patients develop benign and malignant tumors with incr...
Saved in:
| Main Authors: | , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Galenos Publishing House
2008-10-01
|
| Series: | Güncel Pediatri |
| Subjects: | |
| Online Access: | http://www.guncelpediatri.com/yazilar.asp?yaziid=864&sayiid= |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|