61. Dandy – Walker Malformation any recognisable syndrome and these associations together with the classical triadof dandy – walker malformation, are referred to as dandywalker syndrome. http://www.amershamhealth.com/medcyclopaedia/Volume VII/DANDY WALKER MALFORMATI

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Dandy – walker malformation, In classical Dandy-Walker malformation hydrocephalus is considered a complication rather than part of the malformation and though unusual at birth it is present in 75% of patients by 3 months of age and in 90% of patients at the time of diagnosis. The malformation occurs in 1 per 25,000-30,000 births. Walker Warburg syndrome , Dekaban syndrome, cerebro-oculo-muscular syndrome and vermian hypoplasia with colobomata and hepatic fibrosis.Those genetic syndromes in which vermian agenesis is an occasional feature include Meckel-Gruber, Mohr, orofacial digital syndrome type II, Coffin Siris syndrome Smith Lemli Opitz syndrome Ellis van Creveld syndrome Ruvalcaba Myhere Smith syndrome .Other non-Mendelian syndromes in which vermian agenesis may be a feature include Dandy-Walker cyst with facial angioma

62. Congenital Hydrocephaly Associated At Dandy-Walker Syndrome. Case Report And Rev http://www.medigraphic.com/ingles/i-htms/i-pediat/i-sp2000/i-sp00-2/im-sp002g.ht

63. Congenital Hydrocephaly Associated At Dandy-Walker Syndrome. Case Report And Rev Congenital hydrocephaly associated at dandywalker syndrome. Casereport and review. López HJF, García RR, Sánchez VG, Pérez http://www.medigraphic.com/ingles/i-htms/i-pediat/i-sp2000/i-sp00-2/ir-sp002g.ht

López HJF, García RR, Sánchez VG, Pérez ZMA Congenital hydrocephaly associated at Dandy-Walker syndrome. Case report and review Original title: Hidrocefalia congénita asociada a: Síndrome de Dandy-Walker. Revisión e informe de un caso Rev Mex Pediatr 2000; 67 (2): 78-82 ABSTRACT Congenital hydrocephaly is a difficult diagnostic problem, attributable to no hereditary causes, the genetical agents are important, the physiopathologic findings and the subsequent medical management and advices to the parents can confuse its determination. Specifically when uncommunicative congenital hydrocephaly is the result of aqueductal stenosis, other abnormalities association with congenital hydrocephaly must be considered aside; as Dandy-Walker’s Syndrome case. Dandy-Walker’s Syndrome is a malformation of the fourth ventricle and cerebella vermis hypoplasia due to a vermis developmental defect before the embryological differentiation, clinical manifestations tend to prove theirselves during lactation because of skull growing in a progressive way due to hydrocephaly essentially, another congenital encephalic malformations of neuronal migration upsets can appear; the treatment is the ventricles derivation. Key words: Hydrocephaly, vermis hypoplasia, hipertrophy of ventricle.

64. Bombay Hospital Journal - Case Reports - Facial Hemangioma In The association of facial angioma with dandywalker syndrome is rare. Benda CE.The dandy-walker syndrome or the so called atresia of the foramen Magendie. http://www.bhj.org/journal/1998/4001_jan/cr_185.htm

65. Template Page For Individual Syndrome Web Site from thePediatric Database. Mailing List Enquiries. We're glad to welcome......dandywalker syndrome. OMIM Direct Link. Clinical http://georgia.ncl.ac.uk/URODwSMLS/IWS/Ds/DW.html

Dandy-Walker Syndrome OMIM Direct Link Clinical Description from the Pediatric Database Mailing List Enquiries We're glad to welcome you to this framework home page for Dandy-Walker Syndrome, and we want to encourage you to contribute and receive support from others so touched, around the world. Return to D's Return to Index Link to Webmaster

66. Dandy-Walker Syndrome dandywalker syndrome. dandy-walker syndrome - National Institutesof Health. Copyright © 2001 MDinteractive, LLC. • All Rights http://mdinteractive.com/v2/dandy.html

Dandy-Walker Syndrome Dandy-Walker Syndrome - National Institutes of Health

67. MDinteractive--Neurology DRUG DATABASE. YOUR LIFE EXPECTANCY. STAY FIT. SEARCH. MEDLINE. MDinteractive.dandywalker syndrome dandy-walker syndrome - National Institutes of Health. http://mdinteractive.com/dandy.htm

MEDICAL RECORDS I'm a new user: Sign me up Username: Passphrase: SPECIALTIES INTERNAL MEDICINE PEDIATRICS SURGERY OTHER SPECIALTIES GENERAL INFO MEDICAL NEWS FIND PHYSICIAN DRUG DATABASE YOUR LIFE EXPECTANCY ... STAY FIT SEARCH MEDLINE MD interactive Dandy-Walker Syndrome Dandy-Walker Syndrome - National Institutes of Health Send Us Suggestions Free Web Email Free Internet Hard Drive - 20 MB Free Hosting of Your Webpages ... MDinteractive Home

68. Alzhheimer dandywalker syndrome. dandy-walker syndrome - National Institutes ofHealth. Back Tufts Neurology Homepage Please send your webpages http://tuftsneurology.org/webres/dandy.htm

Dandy-Walker Syndrome Dandy-Walker Syndrome - National Institutes of Health Back Tufts Neurology Homepage Please send your webpages comments or questions to: Paulo Andre, MD Last updated January 1,, 1999

69. Indian Pediatrics -Case Reports Fig. 3. CT scan revealed a highly placed and moderately enlarged third ventricleand enlarged fourth ventricle typical of dandywalker syndrome. Discussion. http://www.indianpediatrics.net/june2000/june-673-676.htm

Home Past Issue About IP About IAP ... Subscription Case Reports Indian Pediatrics 2000;37: 673-676 Aicardi Syndrome with Dandy-Walker Malformation Jageerhussain M. Dhinagar S. Nadaradjan S. Bhat B.V. From the Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry 605 006, India. Reprint requests: Prof. B. Vishnu Bhat, Professor of Pediatrics, JIPMER, Pondicherry 605 006, India. Manuscript Received: November 16, 1999; Initial review completed: December 22, 1999; Revision Accepted: January 5, 2000 Aicardi et al . in 1965 described 8 cases with a triad of spasm in flexion, callosal agenesis and ocular abnormalities(1). This clinical syndrome now includes other features like vertebral anomalies, cortical heterotopias, hypotonia, mental subnormality, poor life expectancy, characteristic electrophysiological and radiological abnormalities(2). This disorder has been observed usually in females with the exception of two male infants(3). We report a typical case of Aicardi syndrome with Dandy walker malformation which is an unusual, association. Case Report A 7-month-old girl presented to us with infantile spasm since the age of two months. She was born by an uncomplicated normal vaginal delivery at term to a primigravida mother. The parents were non-consanguineous and there was no significant antenatal illness. The symptoms started initially with myoclonic jerks and occasional generalized tonic clonic convulsions. Her examination revealed marked hypotonia, micro-ophthalmia of right eye, microcephaly (

70. Mioti: Medical Condition NINDS dandywalker syndrome Information Page. Information from the National Instituteof Neurological Disorders and Stroke. OMIM dandy-walker syndrome. http://www.mioti.com/cat/condition/condition.asp?Cat=DandyWalker

71. Syndrome DB - Table Of Contents D. dandywalker cyst dandy-walker malformation (DWM) dandy-walker malformation-basalganglia disease-seizures syndrome dandy-walker syndrome (DWS) dandy-walker http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_d.html

Multiple Congenital Anomaly/Mental Retardation Syndromes Table of Contents Return to Entry Page A B C ... Z D Dandy-Walker cyst Dandy-Walker malformation (DWM) Dandy-Walker malformation-basal ganglia disease-seizures syndrome Dandy-Walker syndrome (DWS) ... U.S. National Library of Medicine , 8600 Rockville Pike, Bethesda, MD 20894 National Institutes of Health Privacy Accessibility Last updated: 20 November 2001

72. Hydrocephalus Association dandywalker syndrome In the dandy-walker syndrome, the fourth ventricleis enlarged because of partial or complete closure of its outlets. http://www.hydroassoc.org/information/infant.html

Hydrocephalus in Infants and Children Hydrocephalus in infants and young children is frequently diagnosed at birth or shortly thereafter, but sometimes it is not diagnosed until the child is a little older. With the advent of sophisticated imaging technologies such as magnetic resonance imaging (MRI) and ultrasonography, hydrocephalus can be diagnosed in utero, before the baby is born. Read more about prenatal hydrocephalus Signs and Symptoms of Hydrocephalus In an infant, the most obvious sign of hydrocephalus is an abnormal enlargement of the baby's head. The soft spot (fontanel) may be tense and bulging. The scalp may appear thin and glistening, and the scalp veins may appear to have unnatural fullness (prominence), as well. When you feel your baby's head along the suture lines, you may find that the bones are separated. Symptoms to watch for are vomiting, sleepiness, irritability and downward deviation of the baby's eyes (the sunsetting sign). Toddlers whose sutures have not yet closed also show the signs of head enlargement. Older toddlers and children, once their sutures have closed, will show other symptoms of raised intracranial pressure (ICP) caused by their enlarged ventricles. Often these symptoms include headache, nausea, vomiting and sometimes blurred or double vision. The child might have problems with balance, delayed development in such areas as walking or talking, or poor coordination. As with infants, a child may be more irritable or tired than normal. The child may show a change in personality or be unable to concentrate or remember things, and their school performance may decline. Older children may have difficulty waking up and staying awake. While at times the symptoms are very noticeable, other times they can be very subtle and progress so slowly that only in retrospect are they appreciated.

73. NORD - National Organization For Rare Disorders, Inc. walker Malformation DWM; dandywalker Cyst; dandy-walker Deformity;dandy-walker syndrome; Hydrocephalus, Internal, dandy-walker Type; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Dandy Walker

74. MeSH-D Terms Associated To MeSH-C Term Dandy-Walker Syndrome MeSHD terms associated to MeSH-C term dandy-walker syndrome, G2DHome. The number indicates the strength of the association of the http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Dandy-Walker_Syndrome:unknown

75. Cerebellar Disorders In the dandywalker syndrome (not to be confused with dandy's syndrome, indicatingbilateral vestibular loss), there is partial or complete agenesis of the http://www.tchain.com/otoneurology/disorders/central/cerebellar.htm

Cerebellar Disorders Timothy C. Hain, MD Return to Education Index Last update: 6/26/01. This page is meant to provide a general outline of cerebellar disorders. More specific and detailed material is found in links. What is the Cerebellum and what does it do ? The cerebellum is part of the brain. It lies under the cerebrum, towards the back, behind the brainstem and above the brainstem. The cerebellum is largely involved in "coordination". Persons whose cerebellum doesn't work well are generally clumsy and unsteady. The main clinical features of cerebellar disorders include incoordination, imbalance, and troubles with stabilizing eye movements. There are two distinguishable cerebellar syndromes midline and hemispheric. Midline syndromes are characterized by imbalance. Persons are unsteady, they are unable to stand in Romberg with eyes open or closed, and are unable to well perform tandem gait. Severe midline disturbance causes "trunkal ataxia" a syndrome where a person is unable to sit on their bed without steadying themselves. Some persons have "titubation" or a bobbing motion of the head or trunk. Midline cerebellar disturbances also often affect eye movements. There may be nystagmus, ocular dysmetria and poor pursuit. Hemispheric cerebellar syndromes are characterized by incoordination of the limbs. There may be decomposition of movement, dysmetria, and rebound. Dysdiadochokinesis is the irregular performance of rapid alternating movements. Intention tremors may be present on an attempt to touch an object. A kinetic tremor may be present in motion. The finger-to-nose and heel-to-knee tests are classic tests of hemispheric cerebellar dysfunction. While reflexes may be depressed initially with hemispheric cerebellar syndromes, this cannot be counted on. Speech may be dysarthric, scanning, or have irregular emphasis on syllables.

76. Walker-Warburg Syndrome - OBGYN.net Ultrasound Images walkerWarburg syndrome Transverse plane of fetal head. agensis of the cerbellarvermis (dandy-walker), hydrocephalus, lissencephalous, and agensis of the http://www.obgyn.net/us/us_images/obgynimages/danwalk.htm

Walker-Warburg Syndrome Transverse plane of fetal head. agensis of the cerbellar vermis (Dandy-Walker), hydrocephalus, lissencephalous, and agensis of the corpus callosum. Neonate has a seizure disorder. Submitted by Terry DuBose, MS, RDMS Walker-Warburg Syndrome Coronal plane of fetal head. agensis of the cerbellar vermis (Dandy-Walker), hydrocephalus, lissencephalous, and agensis of the corpus callosum. Neonate has a seizure disorder. Submitted by Terry DuBose, MS, RDMS Add your Image

77. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE dandywalker MALFORMATION dandy-walker SYNDROOM dandy-walker syndromedandy-walker MALFORMATION. dandy-walker syndrome - Baylor Coll. http://www.vada.nl/medisch/meddad.htm

VADA - GEZONDHEID en ZIEKTE HEALTH and DISEASE DA - DD Last update: 26-01-2003 ATTENTION Patienten en leken die raadgevingen/adviezen/informatie zoeken via deze verzameling links wordt dringend geadviseerd de verzamelde informatie te bespreken met de (behandelend) arts/specialist/hulpverlener. Patients and lay persons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. DACTYLIES DEFECTS of the FINGERS ACROSYNDACTYLY UNILATERAL ADACTYLIA BRACHYDACTYLY VENTRUTO DIGIROLAMO FESTA SYNDROME BRACHYSYNDACTYLY CAMPTOBRACHYDACTYLY CAMPTODACTYLY SYNDROME CLINODACTYLY ECTRODACTYLY HEXADACTYLY MACRODACTYLY OLIGODACTYLY SYNDACTYLY PERODACTYLY POLYSYNDACTYLY ZYGODACTYLY See also: VINGERS FINGERS Syndactyly Release Approaches To Differential Diagnosis In Musculoskeletal Imaging: Skeletal Dysplasias Dactylies (defects of the fingers) Clinodactyly and Camptodactyly Ectrodactyly etc. Acrosyndactyly Acrosyndactyly Unilateral Adactyly Adactylia unilateral dominant Adactylia, unilateral

78. Walsh Lab Laboratory - Family Pages - Walker Warburg Syndrome the cerebellum. Sometimes, children with walker Warburg syndrome willbe described with a dandywalker malformation. dandy-walker http://www.bidmc.harvard.edu/neurology/walshlab/walker.warburg.htm

Walker Warburg Syndrome The association of hydrocephalus with lissencephaly and eye abnormalities was first described by Walker in 1942. Later, Warburg reported that this syndrome was inherited as an autosomal recessive disorder, meaning that it occurs when an individual has received 2 malfunctioning copies of a gene, one from each parent. Over time, we have learned more about the specific malformations present in what is now known as the Walker Warburg Syndrome. Since the original description of Walker Warburg Syndrome in 1942, we have discovered that most children have a muscular dystrophy in addition to the eye and brain findings. This muscular dystrophy presents as significantly low muscle tone with poor reflexes. It can be detected by measuring the level of some muscle enzymes. As with other types of lissencephaly, there is a range of severity with some children having severe illness and others having milder Walker Warburg Syndrome. Some children with severe Walker Warburg Syndrome die in the 1st year of life while those with mild Walker Warburg Syndrome may do much better.

79. Dandy-Walkers Syndrom - Små Och Mindre Kända Handikappgrupper The dandywalker syndrome. Neurology 1972; 22 771-780. The dandy-walker syndromea clinico-pathological study of 28 cases. Neurology 1972; 22 771-780. http://www.sos.se/smkh/2000-29-111/2000-29-111.htm

Socialstyrelsen 106 30 Stockholm e-post Socialstyrelsen klassificerar sin utgivning i olika dokumenttyper Dandy-Walkers syndrom Sjukdom/skada/diagnos Orsak till sjukdomen/skadan Symtom Diagnostik ... Databasreferenser Dokumentdatum: 2000-12-06 HTML-version 1.3 Socialstyrelsen Detta är ett utdrag ur Socialstyrelsens kunskapsdatabas om små och mindre kända handikappgrupper. Med små och mindre kända handikappgrupper avses ovanliga sjukdomar/skador som leder till omfattande funktionshinder och som finns hos högst 100 personer per miljon invånare. Syftet med databasen är att ge aktuell information om små och mindre kända handikappgrupper och om det stöd och den service som dessa grupper behöver. För ytterligare information om aktuell diagnos hänvisas till informationsmaterial, litteratur och databaser som anges under resp diagnos. Sjukdom/skada/diagnos Figur: Hjärnan i genomskärning sedd uppifrån Orsak till sjukdomen/skadan Symtom Diagnostik Praktiska tips Resurspersoner Kurser, erfarenhetsutbyte, rekreation fub@fub.se

80. Cleveland Clinic Health System - Health Information Search Results The following information is available for the topic dandywalker syndrome. Please select one. , dandy-walker syndrome. New Search. http://www.cchs.net/health/getcontents.asp?DocID=do-query&TopicId=1293

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