81. Individual Syndrome Web Site Template Page Cornelia de lange syndrome. OMIM Citation Direct Link. Pediatric Database Entry. http://georgia.ncl.ac.uk/URODwSMLS/IWS/Cs/CdL.html

Cornelia de Lange Syndrome OMIM Citation Direct Link Pediatric Database Entry Cornelia de Lange Syndrome Foundation, Inc. Cornelia de Lange Syndrome Pages at Family Village, University of Wisconsin We wish these organisations every success as they continue to educate and support those touched by this syndrome. Return to C's Return to Index Link to Webmaster

82. Other Disabilities And Syndromes Cornelia de lange syndrome (CdLS). CdLS Foundation Outreach A GlobalCommunity United by Cornelia de lange syndrome Dissociation. http://ani.autistics.org/other_specific.html

Specific Disabilities and Syndromes This document is provided as a public information source. The inclusion of any specific link does not necessarily imply that Autism Network International supports the views expressed in the linked web site, and the exclusion of any specific link does not necessarily imply that Autism Network International does not support the views expressed in the unlinked site. Document contents Attention Deficit Disorder (ADD) Cornelia de Lange Syndrome (CdLS) Dissociation Fragile X Syndrome ... Williams Syndrome Attention Deficit Disorder (ADD) Attention Deficit Disorders (ADD) FAQ v1.2 "An Internet FAQ for parents and teachers of ADD diagnosed children." Children and Adults with Attention Deficit Disorder "Children and Adults with Attention Deficit Disorders (CH.A.D.D.) is a nonprofit parent-based organization formed to better the lives of individuals with attention deficit disorders and those who care for them." Cornelia de Lange Syndrome (CdLS) CdLS Foundation Outreach "A Global Community United by Cornelia de Lange Syndrome" Dissociation alt.support.dissociation FAQs

83. MEDLINEplus: Birth Defects Facing the Challenges A Guide to Cornelia de lange syndrome (Corneliade lange syndrome Foundation) Also available in Spanish; http://www.nlm.nih.gov/medlineplus/birthdefects.html

Skip navigation Other health topics: A B C D ... List of All Topics Birth Defects Contents of this page: News From the NIH General/Overviews Anatomy/Physiology ... Statistics Search MEDLINE for recent research articles on Birth Defects You may also be interested in these MEDLINEplus related pages: Cleft Lip and Palate Congenital Heart Disease Down Syndrome Facial Injuries and Disorders ... Genetics/Birth Defects Latest News Birth Defects Linked to Mega-Progesterone (03/21/2003, United Press International) Popular Supplement Causes Mutations (03/18/2003, United Press International) From the National Institutes of Health Jablonski's Multiple Congenital Anomaly/Mental Retardation Syndromes Database (National Library of Medicine) General/Overviews Birth Defects (March of Dimes Birth Defects Foundation) Also available in: Spanish Birth Defects (Nemours Foundation) Birth Defects (American College of Obstetricians and Gynecologists) Descriptions of Leading Categories of Birth Defects (March of Dimes Birth Defects Foundation) Anatomy/Physiology Genes and Birth Defects: Common Forms of Inheritance (March of Dimes Birth Defects Foundation) Late-Appearing Defects (March of Dimes Birth Defects Foundation) Multifactorial Inheritance (March of Dimes Birth Defects Foundation) Clinical Trials ClinicalTrials.gov: Abnormalities

84. WebRing: Hub About this Ring. A ring of web sites dedicated to Cornelia de lange syndrome. Teresa'sPlace This site is about Teresa who has Cornelia de lange syndrome. http://d.webring.com/hub?ring=cdlskids

85. Directory :: Look.com Cornelia de lange syndrome (4) Sites. Baylee's Web Suite Cornelia de lange syndromeSpecially geared towards new parents, family and friends of CdLS children. http://www.look.com/searchroute/directorysearch.asp?p=594624

86. WebGuest - Open Directory : Health : Conditions And Diseases : Neurological Diso Top Health Conditions and Diseases Neurological Disorders ChromosomalCornelia de lange syndrome (4). See also Health Conditions http://directory.webguest.com/index.cgi/Health/Conditions_and_Diseases/Neurologi

Browse thru 1000's of books about health, mind and body: About Us Privacy Statement Acceptable Use Policy Legal Notices ... Contact Us the entire directory only in Chromosomal/Cornelia_De_Lange_Syndrome Top Health Conditions and Diseases Neurological Disorders ... Chromosomal : Cornelia De Lange Syndrome See also: Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Rare Disorders Sites: Baylee's Web Suite: Cornelia de Lange Syndrome - Specially geared towards new parents, family and friends of CdLS children. Information about the disease as well as Baylee's personal progress. The CaF Directory - A description of Cornelia de Lange syndrome, its inheritance patterns and pre-natal diagnosis. NORD - Cornelia de Lange Syndrome - Offers the synonyms, a general discussion and further resources. Pediatric Database - A definition of Cornelia de Lange syndrome, the epidemiology, history, clinical features, organ malformations, investigations and management. Last update: 22:46 PT, Thursday, March 28, 2002 Help build the largest human-edited directory on the web.

87. Liens En Déficience Intellectuelle Translate this page Syndrome Cornelia De Lange (Cornelia de lange syndrome). Cornelia De Langesyndrome foundation. Baylee's web suite. Références intéressantes. http://www.er.uqam.ca/nobel/d341460/liens.htm

(li nks to websites on genetic syndromes and other medical conditions that may cause mental retardation Argininémie (Argininamia) Galactosémie Galactosemia Hydrocéphalie et Spina Bifida hydrocephalus and Spina Bifida Lissencephalie (lissencephaly) Neurofibromatose neurofibromatosis Paralysie Cérébrale Cerebral palsy Phénylcétonurie phenylketonuria Sclérose tubéreuse de Bourneville tuberous sclerosis Trisomies 13, 18 et 21 trisomy 13, 18, 21 Syndrome du bébé secoué (Shaken baby syndrome) Syndrome Alcolo-foetal Foetal alcohol syndrome Syndrome d'Angelman Angelman syndrome ... Syndrome "Cat-Eye" (Cat-eye syndrome) Syndrome Cornelia De Lange (Cornelia de Lange syndrome) Syndrome du Cri du Chat (Cri du chat syndrome) Syndrome de Klinefelter (Klinefelter syndrome) Syndrome Landau-Kleffner (Landau-Kleffner syndrome) Syndrome Langer-Giedion (Langer-Giedion syndrome) Syndrome de Prader-Willi (Prader-Willi Syndrome) Syndrome Smith-Magenis (Smith-Magenis syndrome) ... Syndrome Sturge-Weber (Sturge-Weber syndrome) Syndrome de Turner (Turner syndrome) Syndrome Triplo-X (Triplo-X syndrome) Syndrome de Rett (Rett syndrome) Syndrome de Williams (Williams syndrome) ... Génétique (Genetics) Autisme (autism) Argininémie (argininamia) Yahoo groups: argininémia Description de l'Argininémie (argininamia description) National urea cycle disorders foundation ... Références intéressantes Galactosémie (galactosemia) Galactosemia Ressources and information Parents of galactosemics, Inc.

88. AltaVista Search: Simple Query "Cornelia De Lange" Translate this page Cornelia de lange syndrome Foundation, Inc. Cornelia de lange syndrome Foundation,Inc. Information Available 1. Facts About Cornelia de lange syndrome. http://www.abanet.it/imagitronica/CdL/linkscdl.html

Links sull'argomento: Sindrome Cornelia de Lange In questa pagina potete trovare indirizzi e riferimenti utili per documentarvi e scambiare informazioni sulla Sindrome Cornelia de Lange e gli argomenti relativi. Se avete informazioni indirizzi e riferimenti da fornirci vi invitiamo a spedire un messaggio e-mail con subject: "Indirizzi Cornelia de Lange" e i dati relativi all'indirizzo famigliecdl@abanet.it oppure al webmaster di queste pagine pilingo@abanet.it Indirizzi Utili - ITALIA Associazione Cornelia de Lange Giorgio e Simona Amadori tel. 0721/34519 email: famigliecdl@abanet.it Ambulatorio di Sindromologia e Genetica Clinica II Clinica Pediatrica (Dr. Selicorni) email: ang_sara@yahoo.com Indirizzi Utili - ESTERO AUSTRALIA E ASIA Peter Crawford (President) e-mail: pcrawfor@dynamite.com.au CANADA Bernadette Dalingwater (President) e-mail: cdlscanada@softcom.ca DANIMARCA Frank Skot Anderson (Chair) e-mail: cdlbot@post6.tele.dk

89. De Lange, Syndrome : Arborescences MeSH Translate this page de lange, syndrome. de lange, syndrome C10.597.606.643.210 page CISMeF dumotclef Down, syndrome C10.597.606.643.220 page CISMeF du motclef http://www.chu-rouen.fr/navimesh/navidelangesyndrome.html

De Lange, Syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF système nerveux, maladies manifestations neurologiques manifestations neuro-comportementales retard mental ... Zellweger, syndrome 27 février 2003 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

90. QU'EST-CE QUE LE SYNDROME DE CORNELIA DE LANGE ? Translate this page QU'EST-CE QUE LE syndrome de CORNELIA de lange ? http://orphanet.infobiogen.fr/associations/AFSCDL/AFSCDL.html

QU'EST-CE QUE LE SYNDROME DE CORNELIA DE LANGE ? QU'EST-CE QUE LE SYNDROME DE CORNELIA DE LANGE ? QUELS EN SONT LES SYMPTOMES ET LES MANIFESTATIONS ? EVOLUTION QUE PEUT-ON FAIRE ? ... Nous contacter Le mot syndrome est le terme médical pour désigner un ensemble de signes ou de symptômes reliés, à une cause commune. Le syndrome de Cornelia de Lange (SCDL) vient du nom du Professeur Cornelia de Lange, pédiatre hollandaise, qui a écrit en 1933, un article décrivant deux enfants. Il est parfois appelé le syndrome Brachmann - De Lange, car le Docteur Brachmann décrivit un patient similaire en 1916. C'est un syndrome rare, sa fréquence est de l'ordre de 1 pour 20 000 naissances. Il n'existe pas de critère unique pour établir un diagnostic définitif. La variabilité en est telle que seul un généticien expérimenté ou un médecin familiarisé avec le syndrome peuvent l'évoquer. Y-a-t'il différentes formes d'atteintes ? Oui . De nombreux médecins appellent syndrome Cornelia de Lange "classique" la forme sévère, et "modérée" la forme qui touche les enfants moins sévèrement atteints. Qu'elle est la cause ?

91. Cornelia De Lange's Syndrome Cornelia de lange's syndrome. BASICS deSCRIPTION respiratory failure. ICD9-CM759.8 Cornelia de lange's syndrome Date last updated 9/11/01 http://www.5mcc.com/Assets/SUMMARY/0232.html

92. EnableNet - Enablenet.browse.browse Dis Intellectual and developmental de lange's syndrome de lange's syndrome Matching Resources. Records 12 of 2 Website http://www.enable.net.au/index.cfm?fuseaction=enablenet.browse.browse&catid=2372

93. Indian Pediatrics - Letters To The Editor Letters to the Editor. Indian Pediatrics 2000;37 691. Cornelia deLange syndrome. This is with reference to the article on Cornelia http://www.indianpediatrics.net/june2000/june-691.htm

Home Past Issue About IP About IAP ... Subscription Letters to the Editor Indian Pediatrics 2000;37: 691 Cornelia de Lange Syndrome This is with reference to the article on Cornelia de Lange Syndrome(1) and the subsequent correspondence(2). As Dr. Matthew points out, the occurrence of Cornelia de Lange syndrome in one of two dizygotic twins (in this case a boy and a girl), is indeed what one would expect. However, I would like to address his two subsequent observations. The occurrence of a genetic, autosomal dominant disorder, in two siblings (not monozygotic twins), with both parents being normal, is not necessarily an argument for an environmental cause. Indeed, since the mid 1980s, geneticists have been aware of the phenomenon of gonadal mosaicism in humans. This refers to the presence of more than one germ cell carrying a mutation in the gonad of the individual, when the rest of body (somatic cells, as well as other germ cells) carry normal copies of the gene. This can give rise to exactly the scenario described, with no need to invoke an environmental cause for the syndrome. The converse, monozygotic twins dis-cordant for a disorder, once again may not point to an environmental cause. In the case of a presumed autosomal dominant disorder, such as Cornelia de Lange syndrome(3), this situation has in fact been reported(4,5). A post-zygotic mutation event in one of the twins, very early in gestation, can explain it. This can also be seen in the case of female monozygotic twins with an X-linked disorder, if the X-inactivation pattern is skewed in one of them. In addition, monozygotic twinning- related multiple malformation cases are actually more often discordant than concordant.

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