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Frontal Encephalocele Plus Epilepsy: A Case Report and Review of the Literature

open access: yesBrain Sciences, 2023
An encephalocele is a pathological brain herniation caused by osseous dural defects. Encephaloceles are known to be regions of epileptogenic foci. We describe the case of a 44-year-old woman with refractory epilepsy associated with a frontal skull base ...
Takehiro Uda   +2 more
exaly   +3 more sources

Transsellar trans-sphenoidal encephalocele with cleft lip, cleft palate and agenesis of corpus callosum

open access: yesRadiology Case Reports, 2021
Basal encephalocele is a rare congenital malformation. Among basal encephaloceles, the transsellar, trans-sphenoidal encephalocele is the least common subtype.
Ritesh Lamsal, Raju Paudel
exaly   +3 more sources

Surgical Management of a Canine Encephalocele Communicating with the Nasal Cavity [PDF]

open access: yesAnimals
An encephalocele is a rare congenital or acquired cranial defect characterized by herniation of intracranial tissue through a defect in the skull base. In human and veterinary medicine, these lesions are frequently associated with abnormalities in neural
Jin-Won Lee, Yongsun Kim, Hwi-Yool Kim
doaj   +2 more sources

Polypectomy-induced encephalocele manifested as meningitis and CSF rhinorrhea in a pregnant woman: a case report

open access: yesRadiology Case Reports, 2022
Encephalocele is a protrusion of the intracranial contents through a cranium defect. Encephalocele is divided into primary (congenital) and secondary (acquired) classes.
Amirhossein Soltani, MD   +3 more
doaj   +1 more source

Congenital Interparietal Encephalocele: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Encephalocele is a mesodermal defect in the skull bones and duramater. Parietal encephalocele is a rare congenital anomaly of newborn with variable prognostic value.
Ashok Nayak   +4 more
doaj   +1 more source

Birth prevalence of encephalocele in Africa: a systematic review and meta-analysis

open access: yesBMJ Paediatrics Open, 2021
Objective To identify the birth prevalence of encephalocele in Africa, 2020.Methods We carried out a systematic search of the following databases (PubMed/Medline, PubMed Central, Joanna Briggs Institute (JBI) Library, Cochrane Library, Web of Science ...
Mohammed Oumer   +1 more
doaj   +1 more source

Temporal encephalocele: An epileptogenic focus confirmed by direct intracranial electroencephalography

open access: yesEpilepsy & Behavior Reports, 2023
Several studies have suggested the epileptogenic potential of temporal encephaloceles. However, there is limited literature describing the results of intracranial EEG monitoring for patients with temporal encephaloceles.
Shruti Agashe   +9 more
doaj   +1 more source

Challenging, giant occipital encephalocele in a pediatric saipanese male

open access: yesClinical Case Reports, 2023
Key Clinical Message Giant occipital encephalocele is a rare form of congenital anomaly that involves protrusion of brain tissue (greater in size than the patient's cranial cavity) from a defect in the skull.
Joshua Loya   +3 more
doaj   +1 more source

Surgical Management and Early Outcome of Encephalocele

open access: yesJournal of Nobel Medical College, 2021
Background: There are limited studies pertaining to management of encephalocele in Nepal. So the present study seems justifiable to bridge the gap in the literature on encephalocele from Nepal on its clinical profile and early outcome. This study aims to
Prakash Kafle   +8 more
doaj   +1 more source

Unveiling a rare aetiology of secondary acquired nasolacrimal duct obstruction: A case of morning glory syndrome with contralateral naso-ethmoidal encephalocele

open access: yesIndian Journal of Ophthalmology. Case Reports, 2021
Morning Glory Syndrome (MGS) is a well-established association of basal encephalocele and usually presents with midline cranio-facial anomalies. 45-year-old female presented with Secondary Acquired Nasolacrimal Duct Obstruction (SANDO) in left eye.
Muthukrishnan Vallinayagam   +3 more
doaj   +1 more source

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