21. ÃÈÄÐÎÑÈÐÈÍÃÎÌÈÅËÈß (ÝÒÈÎÏÀÒÎÃÅÍÅÇ, ÊËÈÍÈÊÀ hydrosyringomyelia ETIOLOGY, PATHOGENESIS, CLINIC AND NEUROSURGICALASPECTS OF TREATMENT. VV Kopanitza. Summary. Today there is still http://www.umj.kiev.ua/arhiv/20/5.asp

HYDROSYRINGOMYELIA: ETIOLOGY, PATHOGENESIS, CLINIC AND NEUROSURGICAL ASPECTS OF TREATMENT V.V. Kopanitza Summary. Today there is still much unclear in the origin of hydrosyringomyelia. Different conceptions exist as to its etiology and pathogenesis, and a number of suggestions are under discussion. The dysontogenetic theory dominant until the mid-century, attributed the gliosis origination and the spinal cord cavities formation to the embryonal nervous tissue developmental defects. Within the last decades, however, the new research methods came into being, making it possible to detalise the symptomatology and extend the knowledge of the pathogenesis of this severe and progressive central nervous system disease. Key words: hydrosyringomyelia, etiopathogenesis, classification, clinic, surgical treatment. PDF Ðàçìåð, kB Ïðèìåðíîå âðåìÿ âûêà÷êè ïðè ñêîðîñòè 28 800 bps, ñ umj_20_615.pdf Äëÿ ÷òåíèÿ íåîáõîäèìî èñïîëüçîâàòü Adobe Acrobat Reader, êîòîðûé ìîæíî áåñïëàòíî ïîëó÷èòü íà ñåðâåðå ôèðìû Adobe sl="1.3" web-ìàñòåðó

22. Home Page Of Neurochirurgical Department Particular Aspects. Troubles of CSF Circulation (Hydrocephalus, hydrosyringomyelia,Meningoceles); Surgical Treatment of Epilepsy; http://www.md.ucl.ac.be/nech/

Department of Neurosurgery Cliniques Universitaires St-Luc U C atholique de L ouvain Brussels, Belgium Christian RAFTOPOULOS , MD, PhD Staff Specialties Available Residency Training Program Research ... Publications How to contact the Department of Neurosurgery Phone: 32 2 764 1085 Fax: 32 2 764 8961 E-mail: neurosurgery.adm@clin.ucl.ac.be Faculty of medicine home page Page created on the 29th April 1996 by Christian Raftopoulos ,MD, PhD e-mail: raftopoulos@chir.ucl.ac.be (Update on October 17, 2001) STAFF Faculty Christian Raftopoulos , MD, PhD, Professor and Chairman Secrétaire Général de la Société de Neurochirurgie de Langue Française (WWW.SNCLF.com) Christian Thauvoy, MD A third place is vacant. If you want to apply you must belong to the European community and be fluent in French. Resident Alexandra Collard, MD Consultant Neurosurgeons Claude de Nijs, MD Jean-Marie Hotermans, MD Herbert Rooijakkers, MD In training Victor Scordidis, MD Michael Bruneau, MD Najib Ramzi, MD Neurosurgeons in clinical fellowship Imad Jaffan, MD Doctor in research fellowship A. S. Basel, MD

23. Äèàãíîñòèêà è äèôôåðåíöèàëüíàÿ äèàãíîñòèê� Diagnostic and differential diagnostic of hydrosyringomyelia. KopanitsaVV. From the viewpoint of the nervous system general pathology http://www.intermag.kiev.ua/uan/bulet/num9/21.html

 ôîðìàò³ PDF Îòîíåâðîëîãè÷åñêîå èññëåäîâàíè ñ âêëþ÷åíèåì ëàðèíãîñêîïèè è ýëåêòðîíèñòàãìîãðàôèè (ïîçâîëÿåò îïðåäåëèòü óðîâåíü è ñòåïåíü ïîðàæåíèÿ ñòâîëà ãîëîâíîãî ìîçãà, âîâëå÷åíèå ÿäåð V, VIII, IX, X ïàð ÷åðåïíûõ íåðâîâ, ãèïåðòåíçèþ). Ëàìèíýêòîìèÿ ñ ÷ðåñêîæíîé è ïðÿìîé êèñòîãðàôèåé (ïîçâîëÿåò îöåíèòü ôîðìó è âåëè÷èíó ñèðèíãîìèåëèòè÷åñêîé êèñòû è åå ñîîáùåíèå ñ IV æåëóäî÷êîì). ÊÒ è ÌÐÒ, èõ ñî÷åòàíèå ñ êîíòðàñòíûìè ìåòîäàìè èññëåäîâàíèÿ (ïíåâìîìèåëîãðàôèÿ, ïîçèòèâíàÿ ìèåëîãðàôèÿ) ïîçâîëÿþò âûÿâèòü îñíîâíûå ñòðóêòóðíûå ïàòîëîãè÷åñêèå îòêëîíåíèÿ: ãèäðîöåôàëèþ, ýêòîïèþ ìèíäàëèí ìîçæå÷êà è ñòâîëà ìîçãà, îêêëþçèþ IV æåëóäî÷êà, ïîëîñòè â ìîçãå, èõ ôîðìó, ñîîáùåíèå ïîëîñòåé ñ IV æåëóäî÷êîì, óòîëùåíèå è Íà ðàííèõ ýòàïàõ áîëåçíè âûñòóïàþò ïðåæäå âñåãî ðåãèîíàðíûå èçìåíåíèÿ íà ìèêðîöèðêóëÿòîðíîì óðîâíå, ÷òî ìîæíî âûÿâèòü, èñïîëüçóÿ âåãåòàòèâíûå òåñòû, ïðîñòûå è ðåçóëüòàòèâíûå, ýëåêòðîòåðìîìåòðèþ, òåïëîâèäåíèå, èññëåäîâàíèå æèäêèìè êðèñòàëëàìè è ìåòîäû, õàðàêòåðèçóþùèå ñîñóäèñòóþ ïðîíèöàåìîñòü. Î çàèíòåðåñîâàííîñòè áîëåå âûñîêèõ îòäåëîâ ãîëîâíîãî ìîçãà, â ÷àñòíîñòè ãèïîòàëÿìóñà, áóäóò ñâèäåòåëüñòâîâàòü äàííûå èññëåäîâàíèÿ æèðîâîãî, âîäíîãî, óãëåâîäíîãî îáìåíîâ, ñîñòîÿíèÿ ñîìàòîòðîïíîé ôóíêöèè ãèïîôèçà ñ ïðîâåäåíèåì òåñòà ñ L-ÄÎÔÀ. Ïðîâåäåíèå áèîõèìè÷åñêèõ è èììóíîëîãè÷åñêèõ èññëåäîâàíèé êðîâè è öåðåáðîñïèíàëüíîé æèäêîñòè è îöåíêà ìîðôîôóíêöèîíàëüíûõ ñâîéñòâ êëåòîê êðîâè ïîçâîëÿþò ñóäèòü î ïðîãðåäèåíòíîñòè ïðîöåññà, ãëóáèíå ìåòàáîëè÷åñêèõ ñäâèãîâ è ñòåïåíè íàðóøåíèÿ èììóííûõ ñâîéñòâ îðãàíèçìà ó áîëüíûõ ãèäðîñèðèíãîìèåëèåé [4,8].

24. Publikationen Kinderheilkunde 1998 Woelfle J Haverkamp F, Comment on Nogues M (1999) Repeated syncopes and extendetpaediatric hydrosyringomyelia. J Neurol Neurosurg Psych 65 (5) 805. http://publ.meb.uni-bonn.de/KIN1998.HTM

Index Publikationen (deutsch) Index Publications (english) Bezugsquellen Impressum Publikationen Kinderheilkunde 1998 Ahrens P Pabelick C Schledt U Behne M Zielen S (Safety axpects of bronchoalveolar lavage in risk patients in childhoodcontinuous end-expiratory pCO2 monitoring). Pneumologie 1998 Mar;52(3):157-60 Albers N Management of recombinant human growth hormone therapy at puberty. Hormone Research 49 (Suppl 2): 58-61 Albers N Management of recombinant human growth hormone therapy at puberty. Horm Res 49 (Suppl 2):58-61 Carbohydrates in human Nutrition. Report of a Joint FAO/WHO expert consultation. FAO food and nutrition paper 66, pp.1-127 Bettendorf M Albers N Bauer J Heinrich UE Linderkamp O Maser Gluth C Longitudinal evaluation of salivary cortisol levels in full-term and preterm neonates. Horm Res 50:303-308 Differential immune response to influenza and pneumococcal vaccination in immunosuppressed patients after heart transplantation. Transplantation, 1998 Nov 27;66(10):1340-7 Hagen v C Noeker M Haverkamp F Kongenitale Hypothyreose: Neuropsychologische und neuromotorische Risiken. Screening Journal 1, 6-13

25. Neurological Syndromes A cervicothoracic syndrome may occur in animals (usually dogs) with hydrosyringomyelia(See Syringomyelia and Hydromyelia), often in association with Chiari http://www.ivis.org/special_books/Braund/braund1/chapter_frm.asp?LA=1

26. [ ¥x¥_ºaÁ`¡E¤p¨à¯«¸g¥~¬ì ] = [ Pediatric Neurosurgery Of VGH Taipe (hydromyelia/syringomyelia/syrinx/hydrosyringomyelia),Hydromyelia (central canal),Syringomyelia ? http://www.vghtpe.gov.tw/~pns/learn/01/01_007.htm

Hydromyelia «ü¯áÅ褤¥¡ºÞ¡]central canal¡^ÂX¤j¡ASyringomyelia ©Î syrinx ¥»¯¸©Ò¦³¹Ï¡B¤å¸ê®Æ§¡ÄÝ­ì§@ªÌ©Ò¦³¡A½Ð¤Å¾Õ¦Û«þ¨©

27. Pediatrix Medical Group - Parent's Guide - Conditions & Diseases hydrosyringomyelia – A split that can occur in the spinal cordNot visible to the eye; Requires MRI or CT Scan to diagnose. The http://www.pediatrix.com/parents/Neonatal_Medicine/Conditions/conditions-ntd.htm

var t = ""; document.write(""); var t = ""; document.write(""); Conditions and Diseases in the NICU Neural Tube Defect (NTD) What is NTD? NTD includes a wide variety of malformations that usually involve the nervous system. They occur in the United States in about 1 of every 500 births. The spectrum of NTD includes: Spina bifida occulta – A defect in the bones that surround the spinal cord Usually the lower back bones Usually does not produce neurologic injury early in life Meningocele – A balloon-like, fluid-filled extension of the meninges The meninges is a very thin membrane that normally surrounds the spinal cord. Usually produces little or no neurologic injury Meningomyelocele – Same as meningocele except it now includes spinal cord tissue Amount of neurologic injury depends on size and location Encephalocele – Similar to meningomyelocele, except it involves the skull and brain Anencephaly – One of the most serious malformations with lack of brain development Hydrosyringomyelia – A split that can occur in the spinal cord Not visible to the eye Requires MRI or CT Scan to diagnose The primary system involved is the nervous system, including the brain and the spinal cord. However, many other organs can be involved. Most common are:

28. SURGICAL MANAGEMENT OF SYRINGOMYELIA ASSOCIATED WITH CHIARI I MALFORMATION patients. Clin Neurol Neurosurg 1029196, 2000; Durham S, Sun P, SchutL Chiari malformations and hydrosyringomyelia. Rev Neurol http://med.ege.edu.tr/norolbil/2000/NBD12000.html

Journal of Neurological Sciences (Turkish) Table of Contents NOROL BIL D 18: 1 , 2001 http://www.med.ege.edu.tr/norolbil/2000/NBD12000.html Clinical Report SURGICAL MANAGEMENT OF SYRINGOMYELIA ASSOCIATED WITH CHIARI I MALFORMATION Efkan COLPAN, Sükrü CAGLAR, Ayse KARATAS, Zafer AYDIN, Yücel KANPOLAT, Ertekin ARASIL, Ahmet ERDOGAN, Cumhur DINCER, Nihat EGEMEN Ankara University, Medical Faculty, Department of Neurosurgery, Ankara, Turkey ABSTRACT Key-words: Chiari I malformation, Syringomyelia, Surgical management Chiari malformasyonlarý muhtemelen birbiri ile iliþkisiz dört tip arka beyin anomalisini kapsamaktadýr. Chiari I malformasyonu bilindiði gibi primer serebellar ektopi, tonsiller herniasyon ve birlikte serebellum kaudal kýsmýnýn ve/veya medulla oblangatanýn kaudale doðru yer deðiþtirmesi ve spinal kanal içerisine girmesi ile oluþmaktadýr. Spinal kord’da syringomiyeli ve hidromiyeli olabilir . Bazý olgular lumboperitoneal ve lumbar ponksiyon sonrasý edinsel olarak görülebilmektedir. Chiari I malformasyonunda spinal kanalda beyin omurilik sývýsý ile dolu kavitasyonlarýn yani syringomyelinin önde gelen sebeplerindendir. Syringomyelinin oluþmasýnda deðiþik mekanizmalar öne sürülmüþtür. Serebrospinal sývýnýn akýmýnýn foramen magnumda intrakraniyal ve intraspinal subaraknoid boþluk arasýnda geçiþinin olmayýþý syringomiyeli oluþma sebepleri arasýnda sayýlmaktadýr. Chiari I malformasyonunda en sýk görülen belirtiler; suboksipital aðrý, kuvvetsizlik, duyu kusuru, ýsý duyusu kaybý, dengesizlik, diplopia v.b þeklinde sýralanabilir. Nörolojik muayenede santral kord sendromu, foramen magnum basýsý sendromu, serebellar sendroma ait bulgular gözlenir. Syringomiyeli’de cerrahi tedavi için çeþitli teknikler önerilmektedir.Bu çalýþmamýzda Chiari I malformasyonu ile birlikte görülen syringomiyeli olgularýnýn cerrahi tedavilerinin sonuçlarý deðerlendirilmiþtir.

29. EMedicine - Spina Bifida : Article By Mark R Foster, MD, PhD Syringomyelia or hydrosyringomyelia is the presence of cavities in the spinalcord, which may be due to the breakdown of gliomatous new formations. http://www.emedicine.com/orthoped/topic557.htm

(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Orthopedic Surgery Spine Spina Bifida Last Updated: March 13, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: spina bifida cystica, spina bifida occulta, SBO, myelomeningocele, myelodysplasia, syringomeningocele, rachischisis posterior, syringomyelocele, diastematomyelia, dysraphia, Arnold-Chiari deformity, craniorachischisis, spondyloschisis AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Indications Relevant Anatomy And Contraindications ... Bibliography Author: Mark R Foster, MD, PhD , Clinical Instructor, Department of Orthopedic Surgery, University of Pittsburgh Mark R Foster, MD, PhD, is a member of the following medical societies: American Academy of Orthopaedic Surgeons American Association for the Advancement of Science American College of Surgeons Eastern Orthopaedic Association ... Orthopaedic Research Society , and Pennsylvania Orthopaedic Association Editor(s): Lee H Riley III, MD

30. EMedicine - Myelomeningocele : Article By Kat Kolaski, MD hydrosyringomyelia is caused by hydrocephalus that results in entry of CSF intothe central canal of the spinal cord, causing dilatation and pressure. http://www.emedicine.com/pmr/topic83.htm

(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Physical Medicine and Rehabilitation Medical Diseases Myelomeningocele Last Updated: May 30, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: open spinal dysraphism, neural tube defect, myelodysplasia, spina bifida, spina bifida cystica, spina bifida aperta, open spina bifida AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Kat Kolaski, MD , Adjunct Clinical Assistant Professor, Department of Pediatrics, University of North Carolina; Director, Pediatric and Adolescent Rehabilitation, Charlotte Institute of Rehabilitation Kat Kolaski, MD, is a member of the following medical societies: American Academy for Cerebral Palsy and Developmental Medicine American Academy of Pediatrics American Academy of Physical Medicine and Rehabilitation , and North Carolina Medical Society Editor(s): Teresa L Massagli, MD

31. H Horner Syndrome; @ Huntington's Disease; @ Hydranecephaly; @ Hydrocephalus;@ hydrosyringomyelia; @ Hyperhidrosis; @ Hyperhomocysteinemia; http://www.ad.com/Health/Conditions_and_Diseases/H/

search Top Categories: Hailey-Hailey Disease @ Hair Loss @ Hairy Leukoplakia @ Halitosis ... @ Hypothyroid AD.COM Web Directory is based on ODP - Open Directory Project data. No proprietary software was used in the development of this web site. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor

32. Developmental CNS Abnormalities 2. Symptomatic Chiari. 3. hydrosyringomyelia. Spinal cord. Compression ofupper segements and associated with hydrosyringomyelia (8090%). http://www.ucch.org/sections/neurosurg/NeuroReview/11-Pediatrics/SpinalDysraphis

Developmental Abnormalities of the Central Nervous System Spinal Dysraphism and Related Conditions Contents Definitions Classification of Spina Bifida Epidemiology of Spina Bifida Etiology of Spina Bifida Pathology Principles of Treatment of Congenital Malformations Spina Bifida Occulta Neural Tube Defects (MC, MMC) Dermal Sinus and Associated Dermoid and Epidermoid Tumors Spinal Lipomas Combined Spina Bifida, Split Cord, Neurenteric Cysts Thickened Filum, Myelocystocoele Caudal Agenesis Encephaloceles Chiari II Malformation Tethered Spinal Cord Definitions Spinal dysraphism . A generic term describing pathologic conditions related to improper closure of the caudal neuropore. Encompasses all conditions associated with spina bifida. Craniorachischisis . Total failure of neurulation. It is the most severe form of spinal dysraphism. There is no dorsal axial skeleton or dermal covering. Myeloschisis . Midline clefting of the spinal cord, partial or complete. Spina bifida cystica . Refers to a meningocele or meningomyelocele. Spina bifida aperta . A defect open to the environment. Neural plaque (or placode ). The dorsal neural tissue contained within the meningomyelocele.

33. ICP Monitors Neurosurg 28353357, 1991. Hoffman HJ. hydrosyringomyelia and its managementin childhood. Neurosurg 21347-351, 1987. Muhonen MG, et al. http://www.ucch.org/sections/neurosurg/NeuroReview/11-Pediatrics/ChiariMalformat

Chiari Malformations Definition Historical Arnold-Chiari malformation Classification of Chiari Malformations Type I Caudal displacement of cerebellar tonsils below foramen magnum. Type II Caudal displacement of the cerebellar vermis, IVth ventricle, and lower brainstem below foramen magnum, associated with myelodysplasia. Type III Caudal displacement of the cerebellum and brainstem into a high cervical meningocele. Type IV Cerebellar hypoplasia. Of questionable relation to the others. Embryology day 24 while the posterior neuropore closes 2-5 days later. As the neural tube closes, three flexures form shaping the cephalic end of the tube. First is the cephalic flexure, placing the forebrain at a right angle to the hindbrain. Then the cervical flexure forms. The pontine flexure forms last (about day 29) and is probably caused by increased growth within the rhombencephalon. Because of the pontine flexure formation, the thin roof of the rhombencephalon becomes creased transversely, and this fold is known as the plica chorioidea. It contains the choroid plexus that will come in direct contact with the ependymal lining, and ultimately correlate with the foramina of Luschka. All of the cerebellum will develop rostral to this line and come to overlie the posterior portion of the ventricular roof as a result of later explosive growth. rhombic lip . The paired cerebellar primordia are pushed upward and medially, meeting in the midline and starting their

34. SpringerLink: Child's Nervous System - Abstract Volume 16 Issue 4 (2000) Pp 222- function, bowel function, renal impairment and hypertension, skin breakdown, epilepsyand the incidence of clinically significant Chiari/hydrosyringomyelia. http://link.springer-ny.com/link/service/journals/00381/bibs/0016004/00160222.ht

Child's Nervous System ISSN: 0256-7040 (printed version) ISSN: 1433-0350 (electronic version) Table of Contents Abstract Volume 16 Issue 4 (2000) pp 222-227 Issues of medical management in adults with spina bifida G. V. McDonnell (1), J. P. McCann (2)(3) (1) Northern Ireland Regional Neurology Service, Royal Victoria Hospital, Belfast, Northern Ireland, UK (2) Clinic for Adults with Spina Bifida and Hydrocephalus (CASBAH), Belfast, Northern Ireland, UK (3) Spinal Injuries Unit, Musgrave Park Hospital, Stockmans' Lane, Belfast, Northern Ireland, UK Tel.: +44-1232-669501, ext. 3041 Fax: +44-1232-263357 Received: 7 October 1999 Abstract Key words Article in PDF format (68 KB) Online publication: April 26, 2000 SpringerLink Helpdesk

35. Chiari I Malformation Can cause symptoms such as headache, balance problems, incontinence and memoryproblems. hydrosyringomyelia a fluid cavity in the spinal cord. http://tribble.missouri.edu/ns/chiari/chiariglossary.htm

The Chiari Clinic Mission Who We Are Location ... Glossary Chiari Glossary Apnea: to stop breathing intermittently, often due to compression on the brainstem or lower cranial nerves Arachnoid: the closest membrane covering the brain, appears to resemble a spider web. There are 3 layers of covering of the brain and spinal cord- the dura, arachnoid and pia. Arachnoiditis: inflammation of the arachnoid Aspirate: inhaling fluids into the lungs. Inability to swallow properly, thereby allowing fluid into the lungs. Asymptomatic: without symptoms. Someone who has no symptoms that can be attributed to a disorder. Ataxia: inability to coordinate movement. Stumbling when walking, or inability to maintain a fluid gait when asked to walk a straight line. Atrophy: wasting away of the muscle, often due to lack of use or inability to exercise a muscle. Atrophic: changes in the muscle that create an appearance of being wasted away Basilar Invagination: the base of the skull and the first cervical vertebra dent inward, causing pressure on the brainstem or upper cervical spinal cord. Catheter: small, soft plastic tube used to drain fluid. A foley catheter is often inserted into the bladder for surgey. A shunt catheter can be inserted into a syrinx or the ventricles.

36. Thieme Medical Publishers : Table Of Contents:DeWald, Spinal Deformities Developmental Spinal Cord Abnormalities; The Spine in Friedrich's Ataxia, CharcotMarie-ToothDisease; Cerebral Palsy, Myelodysplasia, hydrosyringomyelia, Rett http://www.thieme.com/SID2088980784223/productsubpages/toc/pubid-326769985.html

Thieme Medical Publishers Medical Publications DeWald Spinal Deformities Table of Contents I. Gross Anatomy: Surgical Anatomy of the Sacrum and Pelvis; Surgical Anatomy of the Lumbar Spine; Surgical Anatomy of the Thoracic Spine; Surgical Anatomy of the Cervical Spine; Muscles and Ligaments. II. Microanatomy: Development and Maturation of the Spine and Spinal Cord; Microscopic Anatomy of Bone; Macro and Microscopic Anatomy of the Disc and Endplate; Nervous System and Muscle. III. Physiology: Physiology of Bone; Nerve and Muscle Physiology; Pulmonary and Chest Cage Physiology; Electrophysiology; Cerebral Spinal Fluid (CSF) Physiology. IV. Biomechanics: Biomechanics; Biomechanics of the Intervertebral Disc; Spine Testing Modalities. V. Pharmacology: Antibiotic Therapy in Spine Surgery; Osteoporosis: Evaluation and Pharmacologic Treatment; Pharmacologic Agents that Minimize Perioperative Blood Loss...; Common Medications in Spinal Afflictions. VI. Pathology: Pathophysiology of Lumbar Degenerative Disc Disease; Spinal Inflammatory Arthritides; Spinal Neuroarthropathy (Charcot's Spine); Pyogenic Vertebral Infection; Coagulation Disorders in Spine Surgery; Blood Conservation Strategies in Spine Surgery; Management of Metastatic Disease to the Spine. VII. Clinical Evaluation: Evaluation of the Patient with Congenital Spine Deformity; Clinical Evaluation of the Patient with a Spine Deformity; Clinical Evaluation for Neuromuscular Scoliosis and Kyphosis; Evaluation of Back Pain in the Spinal Deformity Patient.

37. Zentrum Für Kinderheilkunde Der Universität Bonn - Wissenschaftliche Publikati Translate this page Woelfle J, Haverkamp F (1998) Comment on Nogues M (1998) Repeated syncopes andextendet paediatric hydrosyringomyelia. J Neurol Neurosurg Psych 65 (5) 805. http://www.meb.uni-bonn.de/kinder/publik.html

Wissenschaftliche Publikationen 1993-2000 der Abteilung für allgemeine Pädiatrie und Poliklinik des Zentrums für Kinderheilkunde der Universität Bonn Adenauerallee 119, D-53113 Bonn, Tel 49-228-2873213, Fax 49-228-2873314 Publikationen 1993 - 1997 Albani M, Gumermuth G, Doose H, Elger C, Fichsel H, Hanefeld F, Heyer R, Jacobi G, Kruse R, Lipinski C, Nolte R, Palm D, Penin H. Rating D, Ritz A, Scollo-Lavizzari G, Speckmann E, Scheffner D, Weinmann HM (1991) Standardtherapien der Epilepsien im Kindes- und Jugendalter. I. Fieberkrämpfe, Epilepsie-Blätter 4, 17-18 Albani M, Gumermuth G, Doose H, Elger C, Fichsel H, Hanefeld F, Heyer R, Jacobi G, Kruse R, Lipinski C, Nolte R, Palm D, Penin H. Rating D, Ritz A, Scollo-Lavizzari G, Speckmann E, Scheffner D, Weinmann HM (1991) Standardtherapien der Epilepsien im Kindes- und Jugendalter. II. West-Syndrom (BNS-Krämpfe, infantile spasms), Epilepsie-Blätter 4, 19-20 Albani M, Gumermuth G, Doose H, Elger C, Fichsel H, Hanefeld F, Heyer R, Jacobi G, Kruse R, Lipinski C, Nolte R, Palm D, Penin H. Rating D, Ritz A, Scollo-Lavizzari G, Speckmann E, Scheffner D, Weinmann HM (1991) Standardtherapien der Epilepsien im Kindes- und Jugendalter. III. Juvenile Epilepsie mit generalisierten tonisch-klonischen Anfällen (Aufwach-Epilepsie), Epilepsie-Blätter 4, 20-21

38. Division Of Neurosurgery developed. One is Chiari malformation and hydrosyringomyelia. Patientsoften present in the pediatric age group with scoliosis. http://www.childrenshospitalla.org/neurosurgery2.html

Division of Neurosurgery Brain and Spinal Cord Tumors Optimal treatment of brain tumors requires a sophisticated, coordinated multidisciplinary treatment approach - one that calls upon the expertise not only of neurosurgeons, but neurologists, neuroradiologists, neuropathologists, neuro-oncologists, neuro-ophthalmologists, radiation therapists, psychologists, rehabilitation therapists and clinical nurse specialists. CHLA physicians provide coordinated expertise in all of these areas allowing for optimum treatment of children with tumors. Every year, Division surgeons perform approximately 100 operations for tumors on the brain or spine. All of the latest technical equipment is available to provide the most advanced approach to surgical resection of tumors of the central nervous system. An excellent ICU staff is available to help with management of the immediate post-operative care of these patients. Physicians at CHLA are active and leading participants in the Childrens Cancer Group wherein new modes of therapy are continually being evaluated to improve outcomes for our patients with these devastating diseases. Our outcome statistics exceed or match any other program within the United States and beyond.

39. Instability Of The Cervical Spine And Neurological Involvement the neck is extended. There is no evidence of Chiari malformation,diastematomyelia, or hydrosyringomyelia. Active extension of http://www.simmonsortho.com/literature/Instability_of_the_Cervical_Sp/instabilit

Back to Physician Literature Instability of the Cervical Spine and Neurological Involvement in Klippel-Feil Syndrome A CASE REPORT* BY J. E. HALL, M.D., E. D. SIMMONS, M.D., F.R.C.S.(C), K. DANYLCHUK, M.D., AND P. D. BARNES, M.D., BOSTON, MASSACHUSETTS From the Department of Orthopaedic Surgery, Children's Hospital, Harvard Medical School, Boston The clinical and pathological findings in patients who Klippel-Feil syndrome have been well documented . The original classic triad of features was described by Klippel and Feil as a short neck, a low hairline posteriorly, and a restricted range of motion of the neck. Since then, other musculoskeletal defects, as well as genitourinary, auditory, cardiopulmonary, and neurological anomalies, have been found to be frequently associated with Kipple-Feil syndrome . The various anomalies of cervical spine have been further characterized and defined . Most patients who have this syndrome are first seen with restricted motion of the neck, torticollis, webbing of the neck, or Sprengel deformity

40. MUMS List Of Disorders - H central spinal cord) (2); Hydronephrosis (44) *; hydrosyringomyelia ArnoldChiari (1); Hyper IGA Syndrome (2); Hyper IGE Syndrome http://www.netnet.net/mums/mum_h.htm

Return to MUMS Home Page MUMS: List of Disorders H Number in parentheses indicates number of matches. indicates there is a support group which covers that diagnosis. HELLP Syndrome (4) HIB Vaccine (bad reactions) (6)* HMG CoAlyase Deficiency (1) * Hair, Atrichia Congenita (1) Hair, Monileth (1) Hajdu-Cheney Syndrome (3) www.hajducheneysyndrome.com Hall-Pallister Syndrome (Pallister-Hall) (1)* Hallermann-Streiff Syndrome (6) * Hallervorden-Spatz Disease (13)* Hallucinations (6) Hands; 1 Foot Absent (1) * Hands Missing (Congenital) (5) * http://www.amp-info.net/ Hanging, Anoxic brain damage from (5) Hanhart Syndrome (2) Happy Puppet Syndrome (Angelman Syndrome) (69)* Hartnup Disorder (3) Hashimoto's Syndrome (2) Hay-Wells Syndrome (3) * Head Trauma (26)* Headaches, Chronic Non-Progressive, caused by stress (1) Hearing Impairment (439)* Hearing Loss-Unilateral (14)* Heart Block, Congenital (3)* Heart Defects (1231)* Heart Transplant (5) * Heart Transplant pending (8) Hemangiectatic Hypertrophy (Klippel-Trenaunay Syndrome) (28) ** Hemangioma, Cavernous and Capillary (9) *

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