1. NORD - National Organization For Rare Disorders, Inc. Offers the synonyms, a general discussion and further resources. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Cornelia de L

2. CdLS USA Foundation: Cornelia De Lange Syndrome The Cornelia de lange syndrome (CdLS) Foundation is a nonprofit 501 (c) (3) voluntary health organization based in Avon, Connecticut (USA). http://www.cdlsusa.org/

Your browser does not support script A Community united by Cornelia de Lange Syndrome Welcome to the official web site of the CdLS-USA Foundation. We hope the information on this site will shed light on any questions you may have about Cornelia de Lange Syndrome and this Foundation. The CdLS Foundation is a family support organization which exists to reach out, provide help and offer hope to everyone touched by this genetic condition. Our primary purpose is to offer support on a personal basis and we encourage you to let us know how we can help you and the person in your life with CdLS. Please join us and support our mission of Reaching out, Providing help and Giving hope to everyone touched by CdLS. Schedule Your CdLS Event Online Did you know that you can schedule your CdLS Awareness Activity or CdLS Gathering online? The online forms are accessible via the links below: NEWS Click above to connect with a family in your area FEATURED ARTICLES: Reflux — Managing a Common Concern GI Distress — Diverse Manifestations WWW CdLSusa.org

3. CORNELIA DE LANGE SYNDROME : Contact A Family - For Families With Disabled Child printer friendly, CORNELIA de lange syndrome, Cornelia de lange syndrome (CDLS) is rare and affects between 1 in 40,000 and 1 in 100,000 babies born. http://www.cafamily.org.uk/Direct/c72.html

printer friendly CORNELIA DE LANGE SYNDROME home more about us in your area conditions information ... how you can help search this site Did you find this page helpful? yes no Cornelia de Lange: Brachmann-de Lange; De Lange I syndrome; Amsterdam dwarfism Cornelia de Lange syndrome (CDLS) is rare and affects between 1 in 40,000 and 1 in 100,000 babies born. Children with Cornelia de Lange syndrome have a particular facial appearance and often look like brothers and sisters. They are small at birth and remain small compared to children of the same age. The ability to learn is delayed in children but this varies from mild to severe. Almost all have limb abnormalities which range from small arms to complete absence of the forearms. Feeding and bowel problems, particularly gastro-oesophageal reflux, are also present. In almost all cases the children will have an unusual marbled appearance to the skin on their arms and legs, particularly when they are cold. Some of the children will have psychological and behavioural problems including autistic-like features and self-injury. Other problems including heart problems may also be present.

4. EMedicine - De Lange Syndrome : Article By Krystyna H Chrzanowska, MD, PhD de lange syndrome de lange syndrome is a relatively common multiple congenital anomaly/mental retardation (MCA/MR) disorder of unknown cause. It is entry 122470 in the Online Mendelian contribution, both Brachmann's and de Lange's names have been attached to the syndrome, Brachmann-de lange syndrome (BDLS). Several hundred http://www.emedicine.com/derm/topic722.htm

(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Dermatology Pediatric Diseases de Lange Syndrome Last Updated: December 19, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: Cornelia de Lange syndrome, CDL, CDLS, Brachmann-de Lange syndrome, BDLS, typus degenerativus amstelodamensis, multiple congenital anomaly/mental retardation, MCA/MR, MIM 122470, malformation syndrome AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Krystyna H Chrzanowska, MD, PhD , Head of Genetic Counseling Unit, Associate Professor, Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland Coauthor(s): Camila K Janniger, MD , Chief of Pediatric and Geriatric Dermatology, Clinical Professor, Dermatology and Clinical Associate Professor, Pediatrics, UMDNJ-New Jersey Medical School Editor(s): Albert C Yan, MD

5. Cornelia De Lange Syndrome / Family Village Library Library C D. Cornelia de lange syndrome. Who to Contact. The Cornelia de lange syndrome Foundation, Inc. 302 West Main Street, 100 http://www.familyvillage.wisc.edu/lib_cdls.htm

Cornelia de Lange Syndrome Who to Contact Where to Go to Chat with Others Learn More About It Web Sites ... Search Google for "Cornelia de Lange Syndrome" Who to Contact The Cornelia de Lange Syndrome Foundation, Inc. 302 West Main Street, #100 Avon, CT 06001 860-676-8337 - Fax Web: http://www.cdlsusa.org/ The Cornelia de Lange Syndrome Foundation is a family support organization which exists to reach out, provide help and offer hope to everyone touched by this genetic condition. Our primary purpose is to offer support on a personal basis and we encourage you to let us know how we can help you and the person in your life with CdLS. Where to Go to Chat with Others CDLS-KIDS An e-mail discussion list for parents, caregivers, extended family, and friends of children with CDLS. CDLS On-Line Parent Support Group Learn More About It Facts About Cornelia de Lange Syndrome About CDLS Cornelia de Lange Syndrome information from OMIM Cornelia de Lange Syndrome information from Ped Base Web Sites Cornelia de Lange Syndrome Foundation Web Site Cornelia de Lange Syndrome - UK Cornelia de Lange Syndrome (CdLS) Online Support Group Jessica's Place Amanda's Room Kayla's (Prink) Web Site Back to [ C - D Family Village Home Library Coffee Shop ... Information Last Updated 11/20/2003 by familyvillage@waisman.wisc.edu

6. EMedicine - Cornelia De Lange Syndrome : Article By Mustafa Tekin, MD Cornelia de lange syndrome Cornelia de lange syndrome (CDLS) is a multiple congenital anomaly syndrome characterized by a distinctive facial appearance, prenatal and postnatal growth deficiency http://www.emedicine.com/ped/topic482.htm

(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Cornelia De Lange Syndrome Last Updated: March 7, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: CDLS, Brachmann-de Lange syndrome, de Lange syndrome, Amsterdam syndrome, typus degenerativus amstelodamensis, growth deficiency, feeding difficulties, psychomotor delay, behavioral problems, upper extremity malformation, characteristic facies AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: Mustafa Tekin, MD , Assistant Professor of Pediatrics and Genetics, Division of Pediatric Molecular Pathology and Genetics, Ankara University School of Medicine, Turkey Coauthor(s): Joann Bodurtha, MD, MPH , Associate Chairman, Associate Professor, Department of Human Genetics, Medical College of Virginia Mustafa Tekin, MD, is a member of the following medical societies:

7. Special Child: Disorder Zone Archives - Cornelia De Lange Syndrome Cornelia de lange syndrome. Madalyn Gilchrist. Cornelia de lange syndrome (CdLS) is a disorder that results in several physical and developmental abnormalities. http://www.specialchild.com/archives/dz-010.html

Disorder Zone Archives Cornelia de Lange Syndrome Madalyn Gilchrist Ketchel Clements Introduction Cornelia de Lange syndrome (CdLS) is a disorder that results in several physical and developmental abnormalities. The cause of CdLS is unknown at this time, however, it is thought that the disorder may be of a genetic nature (possibly a faulty gene on chromosome 3). Most cases are sporadic, however, there has been documentation of affected siblings, which would suggest inheritance. It is said to occur in 1 in 10,000 to 1 in 30,000 live births and is found equally in males and females. Although this syndrome is considered rare, experts agree that it is likely underdiagnosed. CdLS was first described in 1916 by Dr. W. Brachmann and was later identified again by Dr. Cornelia de Lange, a Dutch pediatrician, in 1933. Both physicians described children with common symptoms and characteristics (as shown below). Features and Characteristics There are several physical and developmental characteristics that are associated with CdLS, however, not every individual has all the characteristics. The following is a list of the most common traits: Low birth weight (usually under 5 pounds) Delayed growth and small stature Developmental delay Limb differences (sometimes missing limbs or portions of limbs) Small head size (microcephaly) Thin eyebrows which typically meet at midline Long eyelashes Short upturned nose and thin downturned lips Long philtrum Excessive body hair

8. 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. http://www.geocities.com/Heartland/Plains/1508/

9. CdLS USA Foundation: Cornelia De Lange Syndrome The Cornelia de lange syndrome (CdLS) Foundation is a nonprofit 501 (c) (3) voluntary health organization based in Avon, Connecticut (USA). The Foundation provides a host of services that A Community united by. Cornelia de lange syndrome. Welcome to the official web site of the CdLSUSA you may have about Cornelia de lange syndrome and this Foundation. http://www.cdlsoutreach.com/

Your browser does not support script A Community united by Cornelia de Lange Syndrome Welcome to the official web site of the CdLS-USA Foundation. We hope the information on this site will shed light on any questions you may have about Cornelia de Lange Syndrome and this Foundation. The CdLS Foundation is a family support organization which exists to reach out, provide help and offer hope to everyone touched by this genetic condition. Our primary purpose is to offer support on a personal basis and we encourage you to let us know how we can help you and the person in your life with CdLS. Please join us and support our mission of Reaching out, Providing help and Giving hope to everyone touched by CdLS. Schedule Your CdLS Event Online Did you know that you can schedule your CdLS Awareness Activity or CdLS Gathering online? The online forms are accessible via the links below: NEWS Click above to connect with a family in your area FEATURED ARTICLES: Reflux — Managing a Common Concern GI Distress — Diverse Manifestations WWW CdLSusa.org

10. CdLS USA Foundation: Facts About CdLS are also found in some individuals. Top of Page. Why is it called Cornelia de lange syndrome (CdLS)? In 1933, Dr. Cornelia de Lange http://www.cdlsusa.org/about_cdls/faq.html

Your browser does not support script FAQs About CdLS What is a Syndrome? How is CdLS recognized? Why is it called Cornelia de Lange Syndrome (CdLS)? How many people have CdLS? ... If my child has CdLS, what can I expect? What is a Syndrome? "Syndrome" is a medical term for a condition in which there is a collection of signs (observable body changes) and symptoms (problems observed by the patient) recognizable by a doctor's exam. Individuals with a syndrome may not have all of its associated signs and symptoms, but they must have enough to be considered "diagnostic." Conversely, because someone may display some of the signs and symptoms of a syndrome, does not necessarily mean they have it. Top of Page How is CdLS recognized? CdLS is a congenital syndrome, meaning it is present from birth. Most of the signs and symptoms may be recognized at birth or shortly thereafter. A child need not demonstrate each and every sign or symptom for the diagnosis to be made. As with other syndromes, individuals with CdLS strongly resemble one another. Common characteristics include: low birthweight (often under five pounds), slow growth and small stature, and small head size (microcephaly). Typical facial features include thin eyebrows which frequently meet at midline (synophrys), long eyelashes, short upturned nose and thin, downturned lips. Other frequent findings include excessive body hair (hirsutism), small hands and feet, partial joining of the second and third toes, incurved fifth fingers, gastroesophageal reflux, seizures, heart defects, cleft palate, bowel abnormalities, feeding difficulties, and developmental delay. Limb differences, including missing limbs or portions of limbs, usually fingers, hands or forearms, are also found in some individuals.

11. Gene Discovered For Cornelia De Lange Syndrome, A Disabling Genetic Disease c.moreover.com/click/here.pl?x155365540 More results from c.moreover.com CdLS Online Support Group Copyright CdLS Online Support Group All rights reserved Contact us contact@cdlssupport.org Not affiliated with the Cornelia de lange syndrome Foundation. http://c.moreover.com/click/here.pl?r155365540

12. Cornelia De Lange Syndrome Information Diseases Database Cornelia de lange syndrome Information. Search Cornelia de lange syndrome. aka/or. de lange syndrome http://www.diseasesdatabase.com/sieve/item1.asp?glngUserChoice=29651

13. Pediatric Database A definition of Cornelia de lange syndrome, the epidemiology, history, clinical features, organ malformations, investigations and management. http://www.icondata.com/health/pedbase/files/CORNELIA.HTM

14. Cornelia De Lange Syndrome Cornelia de lange syndrome. Cornelia de lange syndrome (CDLS), also known as Bachmannde lange syndrome, is a genetic disorder present from birth. http://rarediseases.about.com/cs/cdls/a/101903.htm

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Rare Diseases C - D Rare Diseases: C ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Stay Current Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Email to a friend Print this page Stay Current Subscribe to the About Rare / Orphan Diseases newsletter. Suggested Reading Internet links on CDLS Elsewhere on the Web CdLS-USA Foundation Most Popular ALD and Lorenzo's Oil The Elephant Man's Bones Reveal Mystery Prune Belly (Eagle-Barrett) Syndrome Progeria Syndromes ... Mad Cow Disease and Humans What's Hot Autoimmune Kidney Disease Tourette Syndrome Christmas Disease Bugs, PANDAS, and Tics ... Dystonia and Botox Injections Cornelia de Lange Syndrome From Mary Kugler Your Guide to Rare / Orphan Diseases Sign up for my Newsletter Distinctive facial features help identify syndrome Symptoms Language and behavior problems Treatment RATE THIS ARTICLE Would you recommend this article?

15. Cornelia De Lange Syndrome Rare / Orphan Diseases, Cornelia de lange syndrome (CDLS) Guide picks. Cornelia de lange syndrome Article describes the syndrome, its diagnosis, and treatment. http://rarediseases.about.com/cs/cdls/

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Home Essentials ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Stay Current Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Cornelia de Lange Syndrome (CDLS) Guide picks Syndrome characterized by facial and upper limb malformations and behavioral problems. Cornelia de Lange Syndrome Article describes the syndrome, its diagnosis, and treatment. From the About.com Guide to Rare/Orphan Diseases. CdLS USA Foundation Site offers information, news, research, newsletter, and links. CdLS Online Support Group Site offers message board, chat, kids' email list, Spanish email list, facts, and links. NORD: Cornelia de Lange Syndrome Brief definition from the National Organization for Rare Disorders (U.S.). Topic Index email to a friend back to top Our Story ... User Agreement

16. Cornelia De Lange Syndrome de lange syndrome information, national and international support groups, clinics with genetic counselors and geneticists de lange syndrome. Cornelia de lange syndrome, BrachmanDeLange. Cornelia http://www.kumc.edu/gec/support/cornelia.html

de Lange syndrome Cornelia de Lange syndrome, Brachman-DeLange Cornelia de Lange Syndrome Foundation 302 West Main Street, #100 Avon, CT 06001 Telephone: 800.223.8355 or 860.676.8166 Fax: 860.676.8337 E-mail: info@cdlsusa.org Web site: www.cdlsusa.org or www.cdlsoutreach.org/ CdLSWorld , international organizations Australasia (Australia, Malaysia, New Zealand, Philippines, Singapore and SE Asia) CdLS Association (Australasia), Inc. 159 Boddington Crescent Australian Capital Territory Kambah 2902 AUSTRALIA E-mail: pcrawfor@dynamite.com.au Phone: 02 62 31 6866 Web site: www.cdlsaus.org/ New South Wales / Capital Territory Coordinator 135 Princes Street Putney, New South Wales 2112 AUSTRALIA E-mail: jrollo@one.net.au Phone: 02 9809 0287 New Zealand 11 Winsomere Circle Westmere, Auckland 2 NEW ZEALAND E-mail: vernon@ptgroup.co.nz Phone: 09 378 0720 Malaysia and Singapore 20-25-2 Angkupuri Condominium Jalan 1/70C off Jalan Bukit Kiara 50480 Kuala Lampur MALAYSIA E-mail: mohdnor@simenet.com

17. DE LANGE SYNDROME Features Listed For de lange syndrome. McKusick 122470. Absent fingers or oligodactyly; Annular pancreas; Cleft palate; Colon, general abnormalities; http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?422

18. Discovery Of Gene For Cornelia De Lange Syndrome Discovery May Lead To Prenatal A team of researchers has discovered a gene for Cornelia de lange syndrome, a disorder consisting of mental retardation, heart defects and a number of physical http://www.sciencedaily.com/releases/2004/05/040519063614.htm

Match: sort by: relevance date Free Services Subscribe by email RSS newsfeeds PDA-friendly format loc="/images/" A A A Find Jobs In: Healthcare Engineering Accounting College Contract / Freelance Customer Service Diversity Engineering Executive Healthcare Hospitality Human Resources Information Tech International Manufacturing Nonprofit Retail All Jobs by Job Type All Jobs by Industry Relocating? Visit: Moving Resources Moving Companies Mortgage Information Mortgage Calculator Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Outdoor Living Source NIH/National Institute Of Child Health And Human Development Date Print this page Email to friend Discovery Of Gene For Cornelia De Lange Syndrome Discovery May Lead To Prenatal Test For Debilitating Disorder A team of researchers has discovered a gene for Cornelia de Lange Syndrome, a disorder consisting of mental retardation, heart defects and a number of physical abnormalities. The researchers were funded by the National Institute of Child Health and Human Development, one of the National Institutes of Health. What's Related Researchers At UT Southwestern Discover Link Between Gene In Rare Disorder And Growth Factor Progress In Mental Retardation Research New Insight Into Fragile X Syndrome: Scientists Identify Possible Link To RNAi related stories Related section: The researchers expect the discovery to speed the development of a prenatal genetic test for the syndrome. A similar test will also be developed to diagnose Cornelia de Lange Syndrome in young children suspected of having the disorder.

19. CdLs UK And Ireland University funded by a lottery grant from The Community Fund have ended a 15year search for the gene that causes the rare Cornelia de lange syndrome. (CdLS). http://www.cdls.org.uk/

Information Centre Facts and basic information about the CdLS syndrome Background Articles about CdLS, growth charts and pictures Diagnostic and Treatment Protocols Medical information relating to the syndrome Email the Scientific Advisory Council, Reaching Out UK RESEARCHERS DISCOVER GENE THAT CAUSES RARE DISORDER A team of researchers from Newcastle University funded by a lottery grant from The Community Fund have ended a 15-year search for the gene that causes the rare Cornelia de Lange Syndrome. (CdLS). Site designed and maintained by Trident Communications

20. CdLs UK And Ireland Why is it called Cornelia de lange syndrome? The syndrome is named after a famous professor of Paediatrics who worked in Amsterdam over 60 years ago. http://www.cdls.org.uk/information/3.htm

Why is it called Cornelia de Lange Syndrome? The syndrome is named after a famous professor of Paediatrics who worked in Amsterdam over 60 years ago. In 1933 she published a paper describing two children with the syndrome. Although these two girls were not related their facial features were so similar that both Professor de Lange and her nursing staff thought that they were the same child. A few years later she described another child with the same facial features as the first two children. There are now hundreds of cases of the syndrome recorded in the medical literature. What does the word syndrome mean? What are the features that go together to make Cornelia de Lange Syndrome? Why is it called Cornelia de Lange Syndrome? Are there other names for the syndrome? ... Is there any research being carried out on the syndrome? Site designed and maintained by Trident Communications

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