Your browser doesn't support javascript.
loading
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
Subject(s)
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

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