Entrez PubMed Two patients who postoperatively developed extensive multiseptated hydrosyringomyeliafollowing surg http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Folder hydrosyringomyelia, hydrosyringomyelia WITH VON HIPPELLINDAU DISEASE Case869276, Spine and Peripheral Nervous System, 0 images. http://www.mypacs.net/cgi-bin/repos/mpv3_repo/wrm/repo-view.pl?cx_subject=794734
All Showcase - Hydrosyringomyelia Current Opinion in Urology Fulltext Volume 12(6) November 2002 There are, however, cases of hydrosyringomyelia that are large and/or progressive The development of hydrosyringomyelia is often associated with active, http://www.allshowcase.com/Health_and_Fitness/Conditions_and_Diseases/H/Hydrosyr
Log In Problems Should patients with significant hydrosyringomyelia be treated differently? More than half the patients in this series had hydrosyringomyelia, http://www.medscape.com/viewarticle/405724
Log In Problems Neurosurgery 37673679, 1995; Hoffman HJ, Neill J, Crone KR, et al hydrosyringomyeliaand its management in childhood. Neurosurgery 21347-351, 1987 http://www.medscape.com/viewarticle/405731_print
Vol 33-1 (1) in The Pathogenesis of Congenital hydrosyringomyelia A Radiological Study . craniocervical anomalies and the development of hydrosyringomyelia. http://www.esnpn.org/joun/33-2/22.htm
Extractions: Vol 33 - ABSTRACT 22 The congenital Cranio-Cervical Anomalies and Their Role in The Pathogenesis of Congenital Hydrosyringomyelia: A Radiological Study. Mohammed Yasser Metwally. Department of neurology and Psychiatry, Ain Shams University ABSTRACT In the present study 20 patients with the clinico-radiological diagnosis of congenital syringomyelia are included. All patients were examined by MRI and CT myelography. Special focus of attention was made on the associated congenital cranio-cervical anomalies with the aim of establishing possible cause-effect relationship between some of the associated cranio-cervical anomalies and the development of hydrosyringomyelia. The single congenital anomaly that was demonstrated in all patients was hindbrain herniation below the level of the foramin magnum (Chiari I malformation was demonstrated in 70% of cases and chiari II malfomation in 30% of cases). Hindbrain herniation induced the following anatomical aberrations; 1) stenosis of the foramin of magnum and the foramin of magendi, and 2) the foramin of magendi was demonstrated below the level of the calamus scriptorious. These anatomical aberrations will redirect the ventricular
Blackwell Synergy - Cookie Absent hydrosyringomyelia may occasionally also be confined to the conus, but in contrastto a dilated ventriculus terminalis, a high incidence of associated http://www.blackwell-synergy.com/doi/abs/10.1034/j.1600-0455.2003.00096.x
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Journal Of Computer Assisted Tomography - UserLogin Diagnosis Chiari I malformation with associated hydrosyringomyelia. Aunt Minnie sPearls In the late nineteenth century, Hans Chiari described a http://www.jcat.org/pt/re/jcat/fulltext.00004728-199705000-00031.htm
Home Page Of Neurochirurgical Department Troubles of CSF Circulation (Hydrocephalus, hydrosyringomyelia, Meningoceles);Surgical Treatment of Epilepsy; Deep Brain Stimulation in Movement Disorders http://www.md.ucl.ac.be/nech/intro.htm
Extractions: SPECIALTIES AVAILABLE Image Guided Neurosurgery (IGNS) Previously with the MKM system of Zeiss and since 2004 with the VectorVision of BrainLab NeuroEndoscopy Deep Brain Stimulation for Abnormal Movements Cranial pathology Spinal pathology Malformative Disorders Cervical Disc Disease and Spondylosis; Lumbar IntervertebralDisc Herniation; Lumbar Spinal Stenosis and Lateral Recess Syndrome
KoreaMed - Basic Search Lipomeningomyelocele with hydrosyringomyelia A Case Report. We hereby report ona newborn infant with a lipomeningomyelocele present with hydrosyringomyelia. http://www.koreamed.org/SearchBasic.php?RID=41081&DT=1&QY=J Korean Soc Neonatol
KoreaMed - Basic Search 2000 Nov;7(2)186188. Korean. 8 Kim MJ, Lee HS. Lipomeningomyelocele withhydrosyringomyelia A Case Report. J Korean Soc Neonatol. 2000 Nov;7(2)181-185. http://www.koreamed.org/SearchBasic.php?QY=J Korean Soc Neonatol [JTI] AND 2000
Hydrosyringomyelia In Demyelinating Diseases Http//www.ncbi.nlm hydrosyringomyelia in demyelinating diseases. http//www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve db=PubMed list_uids=11927108 dopt=Abstract http://www.mult-sclerosis.org/news/Apr2002/MedlineDevicsSyndromeAndMS.html
Extractions: Departamento de Neurologia. Sanatorio Mitre. FLENI. Hospital Britanico. Hospital Sirio Libanes. Hospital Espanol. Buenos Aires. Argentina. Spinal cord cavitation is a frequent finding in optic neuromyelitis (Devic's syndrome) (DS) but it is also, although rarely, observed in patients with multiple sclerosis (MS). The objective of our study was to compare the MRI characteristics of the syringomyelic cavities in 6 patients with DS and 3 patients with MS. All the patients with DS had a relapsing clinical form with normal brain MRI. Spinal MRI revealed unenhanced central cavities which extended more than 3 vertebral bodies and remained unchanged in follow-up studies. Two patients presented multiple cavities.MS patients suffered a relapsing remitting form of the disease, they all had hyperintense T2 enhancing lesions on their spinal MRI. Moreover spinal MRI also revealed non communicating cavities which extended less than 2 vertebral bodies.
Congenital Malformations tonsils into postlat cerv subarachnoid NOT assoc w open spinal dysraphia or brainmalformation IS assoc w basilar skull defects hydrosyringomyelia Chiari II http://www.indyrad.iupui.edu/public/lectures/HTML/neuro/spine/congen.htm
Revista De Neurología - Visualización Del Resumen Chiari malformation and hydrosyringomyelia Susan Durham, Peter Sun, Luis Schut.Rev Neurol Vol.27 Num.156 Pág.0231 Published on 01/08/1998 http://www.revneurol.com/VeureResum.asp?i=i&Ref=97386&Par1=DeAutor.asp&Par2=27&P
Rev. Chil. Neuro-psiquiatr. Vol.38 no.3; Resumen: S0717-92272000000300008 Noncommunicating hydrosyringomyelia has been described in association withseveral types of spinal pathologies, but it has rarely been reported with http://www.scielo.cl/scielo.php?pid=S0717-92272000000300008&script=sci_abstract&
Neurological Syndromes With continuing expansion of the hydrosyringomyelia, ventral horn cells may becomeinvolved leading to neurogenic muscle atrophy and weakness, while dorsal http://www.ivis.org/special_books/Braund/braund1/chapter_frm.asp?LA=1
Karger Publishers There is increasing evidence that hydrosyringomyelia and scoliosis are 20, 10 of 47 children with hydrosyringomyelia presented with scoliosis, http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=
1999 Recalls Answer D hydrosyringomyelia defn coexistence of hydromyelia and syringomyelia.hydro defn a pathologic condition in which there is dilatation of the http://www.radquiz.com/1999_recalls.htm
Extractions: Which of the following is associated with Luckenshcadel skull. myelomeningocele diastematomyelia hydrocephalus other choices not remembered Answer: A: defn: a condition marked by defective calcification of the skull bones, combined with meningocele or encephalocele. This is often seen in Chiari 2 malformation. (Dorlands). -disappears by 4-6 months of age, not a manifestation of hydocephalus as was once thought, represents defective membranous bone formation, but precise etiology unknown, most frequently only the inner table and diploe are involved, dura is thinned over the lacunae, but is of normal thickness over the intervening bony struts,(Swischuck pg 934) Chiari I malformation is associated with: thickened massa intermedia tectal beaking interdigitated falx hydrosyringomyelia Answer: D: Hydrosyringomyelia: defn: coexistence of hydromyelia and syringomyelia: hydro defn: a pathologic condition in which there is dilatation of the central canal of the spinal cord with accumulation of fluid. Syringo defn: a slowly progressive syndrome in which cavitation occurs in the central segments of the spinal cord, may be developmental, 2ndary to tumor, trauma, infarction or hem or idipath, . results in neurological deficits segmental sensory dissociation (dorlands)
