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Neurofibromatosis type II: a rare neurocutaneous syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2007; 17 (6): 376-377
em Inglês | 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
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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Neoplasias Encefálicas / Síndromes Neurocutâneas Tipo de estudo: Relato de Casos Limite: Humanos / Masculino Idioma: Inglês Revista: J. Coll. Physicians Surg. Pak. Ano de publicação: 2007

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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Neoplasias Encefálicas / Síndromes Neurocutâneas Tipo de estudo: Relato de Casos Limite: Humanos / Masculino Idioma: Inglês Revista: J. Coll. Physicians Surg. Pak. Ano de publicação: 2007