Encephalocele
Mostrando 1-12 de 16 artigos, teses e dissertações.
-
1. False Computed Tomography Findings in Bilateral Choanal Atresia
Abstract Introduction Choanal atresia (CA) is a challenging surgical problem defined as a failure in the development of communication between the nasal cavity and nasopharynx. Objective The objective of this study is to describe computed tomography (CT) findings in cases with bilateral choanal atresia. Methods The study involved performing axial and cor
Int. Arch. Otorhinolaryngol.. Publicado em: 2016-06
-
2. Muldisciplinary evaluation of patients with anterior encephalocele: analysis of cranial, brain, neuropsychological and language disorders / Avaliação multidisciplinar de pacientes com encefalocele anterior: análise das alterações cranianas, encefálicas, neuropsicológicas e de linguagem
Objective: To evaluate cranial and brain abnormalities in patients with anterior encephalocele and to analyze relevant aspects to their neuropsychological development, language and quality of live. Model: Transversal study in patients with anterior encephalocele, who underwent a multidisciplinary team assessment (craniofacial, socioeconomic, neuroradiologica
Publicado em: 2008
-
3. Estudo do cariotipo constitucional e dos tecidos envolvidos na lesão de crianças portadoras de defeito do tubo neural (DTN) por meio de analise citogenetica convencional e FISH
The association between chromosomal abnormalities, specially aneuploidies and neural tube defects (NTDs) is well known, principally when NTD is not the only malformation present. Recently, research in animal models, using fluorescence in situ hybridization (FISH) identified aneuploidy in neural tissues. The aims of this work were to identify the frequency of
Publicado em: 2004
-
4. Basal encephalocele and morning glory syndrome.
Basal encephaloceles are often associated with other midline anomalies such as hypertelorism, broad nasal root, cleft lip, and cleft palate. Optic disc anomalies such as pallor, dysplasia, optic pit, coLoboma, and megalopapilla have been reported to occur in patients with basal encephalocele We report a case of a child with a sphenoethmoidal encephalocele an
-
5. Neural tube defects in New South Wales, Australia
Cases of spina bifida cystica, encephalocele, and anencephaly occurring over a 9-year period, 1965 to 1973, in New South Wales, Australia, were identified. A low frequency of 1·1 for spina bifida and encephalocele (SB) and 0·9 for anencephaly (A) was found.
-
6. Nasal endotracheal intubation in a premature infant with a nasal encephalocele.
After a difficult nasal intubation a premature infant leaked cerebrospinal fluid (CSF) from one nostril. After developing bacterial meningitis, the baby was referred for neurosurgical management of the CSF fistula. Transaxial computed tomograms demonstrated a nasal encephalocele, but coronal scans were needed to show the defect in the cribriform plate.
-
7. Encephalocele in the Nasal Region
-
8. Spina Bifida and Anencephalus in Greater London
In order to make comparisons with the findings in a high frequency area, South Wales, with those in a low frequency area, south-east England, a birth frequency and family study was made of all births with neural tube malformations (spina bifida cystica, encephalocele, anencephaly, and iniencephaly) in 32 of the 33 London Boroughs over a 3-year period from 1
-
9. Short report: Encephaloceles in Nigerian Igbos
A survey of surgical specimens submitted to a central laboratory suggests that the Igbos of Nigeria are a further ethnic group in whom the anterior encephalocele is comparatively common.
-
10. Meckel syndrome: what are the minimum diagnostic criteria?
Two sibs are described, the first of whom presented the classic Meckel syndrome triad of encephalocele, postaxial polydactyly, and characteristic renal cystic changes. The second sib had none of these abnormalities, but did show urethral atresia and preaxial polydactyly, two features previously described in some patients with Meckel syndrome. The two cases i
-
11. Meckel's syndrome (dysencephalia splanchno-cystica) in two Pakistani sibs.
A Pakistani couple, who were first cousins once removed through their fathers, and whose mothers were also related, had two liveborn children, a boy and a girl. Both children died within 2 hours of birth with occipital encephalocele, microcephaly, polycystic kidneys, and cystic distension of intrahepatic bile ducts. Both children had normal karyotypes. These
-
12. Pseudoepiphora from cerebrospinal fluid leak: case report.
A 4-year-old tearing child with obstruction of the nasolacrimal duct was treated with dacryocystorhinostomy three years after naso-orbital injury. However, what appeared to be tearing persisted, and meningitis developed. Coronal CT scans demonstrated traumatic encephalocele of the posterior superior orbital roof. A chronic orbital cerebrospinal fluid (CSF) l