MENINGOENCEPHALOCELE

作品数:4被引量:0H指数:0
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相关领域:医药卫生更多>>
相关期刊:《Open Journal of Modern Neurosurgery》《Chinese Medical Journal》《World Journal of Otorhinolaryngology-Head and Neck Surgery》《Chinese Neurosurgical Journal》更多>>
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Pediatric sinonasal and skull base lesions
《World Journal of Otorhinolaryngology-Head and Neck Surgery》2020年第2期118-124,共7页Charles A.Riley Christian P.Soneru Jonathan B.Overdevest Marc L.Otten David A.Gudis 
Pediatric skull base lesions are complex and challenging disorders.Safe and comprehensive management of this diverse group of disorders requires the expertise of an experienced multidisciplinary skull base team.Adult ...
关键词:PEDIATRICS Endoscopic sinus surgery Endoscopic skull base surgery Juvenile nasopharyngeal angiofibroma MENINGOENCEPHALOCELE Pituitary adenoma CRANIOPHARYNGIOMA Clival chordoma CHONDROSARCOMA 
Goldenhar Syndrome with Occipital Meningoencephalocele: A Rare Case
《Open Journal of Modern Neurosurgery》2019年第1期17-22,共6页Mubashshir Ali Ashish Chugh Deepak M. Ranade 
A 7-year-old male patient reported in our neurosurgery OPD with chief complaints of swelling in occipital region. The swelling was gradually increasing in size as per history given by patient’s attendant. Antenatal a...
关键词:GOLDENHAR Syndrome LIMBIC NODULE 
Occipital Meningoencephalocele case report and review of current literature
《Chinese Neurosurgical Journal》2018年第1期55-58,共4页Ahmed Alwahab Adnan Kharsa Alaa Nugud Shomous Nugud 
Background:Meningoencephalocele is a rare congenital anomaly that is characterized by herniation of brain tissue through a defect in skull. Generally, it could be divided by anatomical location of defect to occipital ...
关键词:MENINGOENCEPHALOCELE CONGENITAL CRANIAL MALFORMATION CONGENITAL brain HERNIATION 
Neurofibromatosis complicated with meningoencephalocele:one case report
《Chinese Medical Journal》2007年第23期2151-2152,共2页HUANG Qi-bing WANG Jian-gang LI Xin-gang ZHOU Xu-dong WANG Dong-hai WANG Xin-yu 
Neurofibromatosis type Ⅰ (NF-I) is an autosomal dominant inherited disease caused by a mutated NF-I gene on chromosome 17, which produces inactive neurofibromin. Besides caf6-au-lait spots, and multiple skin neurof...
关键词:neurofibromatosis type  orbital meningoencephalocele 
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