TY  - CHAP
AU  - Hind M. Alkatan
AU  - Sawsan S. Bakry
AU  - Mohammad A. Alabduljabbar
ED  - Francesco Signorelli
ED  - Raffaella Messina
Y1  - 2019-11-07
PY  - 2019
T1  - Ocular Findings in Neurofibromatosis
N2  - Neurofibromatosis, one of the most common genetic disorders, is a group of three conditions—Neurofibromatosis 1, Neurofibromatosis 2 and Schwannomatosis—that share some clinical features, such as the presence of cranial and spinal nerve sheet tumors. However, they differ in type of genetic disorder, age of clinical onset, manifestations, management and prognosis. Due to multisystem involvement, a multidisciplinary treatment approach that includes research is ideal. This book provides a systematic, comprehensive and updated outline of Neurofibromatosis. It is a useful reference for clinicians, researchers and students.
BT  - Neurofibromatosis
SP  - Ch. 5
UR  - https://doi.org/10.5772/intechopen.90021
DO  - 10.5772/intechopen.90021
SN  - 978-1-78985-530-2
PB  - IntechOpen
CY  - Rijeka
Y2  - 2024-04-27
ER  -