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Cornelia De Lange Syndrome: more detail

Cornelia de Lange Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-20
Cornelia de Lange Syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Laith, MD Gulli, Robert, BS Ramirez, 2005
Cornelia de Lange Syndrome / Maple Syrup Urine Disease / Rubinstean-Taybi Syndrome: teaching considerations Part two.: An article from: Palaestra by Robert C. Weber, 2006-01-01
Cornelia de lange syndrome / maple syrup urine disease / Rubinstein-Taybi syndrome: behavior issues, activities, and conclusions.: An article from: Palaestra by Robert C. Weber, 2006-03-22
Cornelia de Lange Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
Love Ella: a mother's story of her daughter with Cornelia de Lange Syndrome by Madeleine Witham, 2006

lists with details

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/

Extractions: 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. 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
Cornelia De Lange Syndrome / Family Village Library
cornelia de lange syndrome. Who to Contact Search Google for "cornelia de lange syndrome" Who to Contact
http://www.familyvillage.wisc.edu/lib_cdls.htm

Extractions: 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. CDLS-KIDS
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
CORNELIA DE LANGE SYNDROME : Contact A Family - For Families With Disabled Child
A description of cornelia de lange syndrome, its inheritance patterns and prenatal diagnosis.
http://www.cafamily.org.uk/Direct/c72.html

Extractions: 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.
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

Extractions: (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 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:
HealthlinkUSA Cornelia De Lange Syndrome Links
Find More on cornelia de lange syndrome. Not finding exactly what you need on%3A cornelia de lange syndrome%3F Why not give
http://www.healthlinkusa.com/82ent.htm
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/
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/

Extractions: 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. 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
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

Extractions: If my child has CdLS, what can I expect? "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 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.
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

Extractions: 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); 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 From Mary Kugler
Special Child: Disorder Zone Archives - Cornelia De Lange Syndrome
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.
http://www.specialchild.com/archives/dz-010.html

Extractions: 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
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/

Extractions: 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); 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)
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
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
Gene Discovered For Cornelia De Lange Syndrome, A Disabling Genetic Disease
c.moreover.com/click/here.pl?x155365540 More results from c.moreover.com 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://c.moreover.com/click/here.pl?r155365540
HealthlinkUSA Cornelia De Lange Syndrome Links
Finding cornelia de lange syndrome is a Click Away at 2020Search.com what you re looking for on%3A cornelia de lange syndrome%3F 2020Search will instantly provide you with
http://www.healthlinkusa.com/cornelia_de_lange_syndrome.htm
Cornelia De Lange Syndrome - Information / Diagnosis / Treatment / Prevention
home neurological disorders chromosomal cornelia de lange syndrome cornelia de lange syndrome. Information Diagnosis Treatment Prevention.
http://www.healthcyclopedia.com/neurological-disorders/chromosomal/cornelia-de-l

Extractions: Web Directory: 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. NORD - Cornelia de Lange Syndrome Offers the synonyms, a general discussion and further resources.
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://www.cdls-support.org/

Extractions: CdLS-KIDS Stay connected! Join our email discussion list. CdLS-AMIGOS Se habla espanol. CdLS-SIBLINGS Email group just for siblings. CdLS-Remembered Support for those who have lost a loved one with CdLS. CHAT Get in on the fun with our weekly chats. MESSAGE BOARD New forum is here! Please visit and post your questions! CdLS FACTS Learn about CdLS. LINKS Links to CdLS home pages and other CdLS-related sites. NEW FAMILIES Letters of support for new CdLS families. INSPIRATION Stories and poems contributed by our members. MEMORIAL PAGE In loving memory of our CdLS angels. Parents sharing adaptive devices that work for their children w/CdLS. TEAM CdLS Raising awareness and funds for the CdLS Foundation. GUESTBOOK Please take a moment and sign our guestbook. Not affiliated with the Cornelia de Lange Syndrome Foundation Welcome to the Cornelia de Lange Syndrome (CdLS) Online Support Group . The group was started by several moms who met regularly online and realized how wonderful it was to have a convenient way of communicating. CdLS is rare enough that finding other parents in close proximity is not always feasible. Now, through this miracle of technology, we can connect with others who have much in common...wherever we may be in the world. We are no longer alone!
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

Extractions: Source NIH/National Institute Of Child Health And Human Development Date Print this page Email to friend 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. 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.
Cornelia De Lange Syndrome; Treatment, Prevention, Cure
cornelia de lange syndromeSearch information from many of the best cornelia de lange syndrome health sites. Quickly find information
http://www.healthlinkusa.com/content/82.html

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