Neurofibromatosis type II: a rare neurocutaneous syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2007; 17 (6): 376-377
Dans Anglais
| 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
Recherche sur Google
Indice:
Méditerranée orientale
Sujet Principal:
Tumeurs du cerveau
/
Syndromes neurocutanés
Type d'étude:
Enquête cas-témoins / Études cas/témoins
Limites du sujet:
Humains
/
Mâle
langue:
Anglais
Texte intégral:
J. Coll. Physicians Surg. Pak.
Année:
2007
Documents relatifs à ce sujet
MEDLINE
...
LILACS
LIS