Neurofibromatosis type II: a rare neurocutaneous syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2007; 17 (6): 376-377
in English
| IMEMR
| ID: emr-94163
ABSTRACT
Neurocutaneous syndromes are heterogeneous group of disorders with abnormalities of central as well as peripheral nervous system. Neurofibromatosis type II [NF-II] is an autosomal dominant neurocutaneous syndrome rarely diagnosed in pediatric population. Diagnosis is based on clinical history and radioimmaging. We present a 14 years old boy with headache and decreased hearing, who turned to be a case of neurofibromatosis type II
Search on Google
Index:
IMEMR (Eastern Mediterranean)
Main subject:
Brain Neoplasms
/
Neurocutaneous Syndromes
Type of study:
Case report
Limits:
Humans
/
Male
Language:
English
Journal:
J. Coll. Physicians Surg. Pak.
Year:
2007
Similar
MEDLINE
...
LILACS
LIS