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         De Lange Syndrome:     more detail
  1. Cornelia de Lange Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-20
  2. Facing the Challenges: A Guide for Caregivers to People with the Comelia De Lange Syndrome by Alan Peaford, 2007-05-01
  3. 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
  4. 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
  5. 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
  6. Cornelia de Lange Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
  7. Love Ella: a mother's story of her daughter with Cornelia de Lange Syndrome by Madeleine Witham, 2006
  8. Delange Syndrome by Joseph M. Berg, 1970-08-20
  9. Into the unknown--first-ever-in-water experience camp for individuals who are cognitively impaired.(care and treatment): An article from: Palaestra by L. Marie Concklin-Malloy, 2006-06-22
  10. Psychiatry : PreTest Self-Assessment & Review, Twelfth Edition by Phil Pan, 2009-04-03

21. HealthlinkUSA Cornelia De Lange Syndrome Links
Find Cornelia de lange syndrome at searchwaves.com. Click here for page 1 of Cornelia de lange syndrome information from the HealthlinkUSA directory.
http://www.healthlinkusa.com/82ent.htm

22. 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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23. Education Protocol For Cornelia De Lange Syndrome
Education Protocol for Cornelia de lange syndrome. Mary Families may struggle to accept the diagnosis of Cornelia de lange syndrome. Shock
http://www.tsbvi.edu/Outreach/seehear/winter00/cornelia.htm
Home Site TOC Site Search Outreach ... Winter 2000 Table of Contents
Education Protocol for Cornelia de Lange Syndrome
Mary T. Morse, Ph.D., Special Education Consultant, Pembroke, New Hampshire Editor s note: Recently I visited the Cornelia de Lange Foundation, Inc. website in search of information for a classroom teacher. I came across this wonderful article, one of the many interesting things available at this site. I would encourage families and professionals who want to learn more about CdLS to visit this site if they haven http://cdlsoutreach.org Cornelia de Lange Syndrome (CdLS) has great variability in its manifestation, from those individuals who are visually recognizable as having CdLS to those who, to the uninitiated observer, display no unusual physical and/or behavioral characteristics. A common characteristic, however, is that numerous infants, preschool and school-age children with CdLS have a range of significant medical and health issues that consume parental physical, emotional and financial energy and the attention of numerous professional disciplines. Many children diagnosed with CdLS also present another set of concerns, namely in the area of communication and behavior. Planning and providing appropriate quality educational services for children who have CdLS must consider the influence and interplay of both sets of issues and concerns. Education is a cultural activity with schools charged to prepare children for the life they will lead in the culture they will live. Education can be thought of as the other side of the coin from the medical and health-related issues and, as such, needs to be addressed simultaneously.

24. Cornelia De Lange Syndrome Conference
Cornelia de lange syndrome Conference. Cornelia de lange syndrome (CdLS) is a genetic disorder that causes mental, physical, and developmental delays.
http://www.tsbvi.edu/Outreach/seehear/fall98/cornelia.htm
Go to Fall 1998 Table of Contents.
Cornelia de Lange Syndrome Conference
By Gwen Solis, Parent, San Antonio, Texas Cornelia de Lange Syndrome (CdLS) is a genetic disorder that causes mental, physical, and developmental delays. Each year families and professionals come together from all over the world for a weekend full of informative workshops, sibling activities, parental bonding and lots of food and fun! This year is the 20th Annual International Conference for the families of children with Cornelia de Lange Syndrome. Our conference will be held at the beautiful Doubletree Hotel in Dallas, Texas from June 24-27, 1999. Each year, no matter where the conference is held, Girl Scout Troop 905/959 from Bogata, New Jersey, raise their own funds to come to the conference and provide loving childcare for the CdLS children, so their families can attend the conference and receive invaluable information. CdLS has its own Scientific Advisory Board. It consists of top medical professionals who specialize in CdLS and attend the conference each year. They range from geneticists, ophthalmologists, ENTs, gastroenterologists, psychologists, orthopedists, dentists, and more. This is always a memorable and important event. If you or anyone you know want to learn more about CdLS or the upcoming conference, please call the CdLS Foundation at (800) 223-8355.

25. 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

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Related Topics: Genetic Disorders Rare Disorders Medical Definition: University of Newcastle-upon-Tyne Medical Dictionary: "Cornelia de Lange syndrome" Health News: Search millions of published articles for news on Cornelia De Lange Syndrome Modern Medicine Aging The Ardell Wellness Report HealthFacts Medical Post Medical Update Men's Health and the National Women's Health Report Note: Subscription required to access the full text of articles. 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.

26. Cornelia De Lange Syndrome
Refer to conditions of use. Cornelia de lange syndrome (Amsterdam Dwarf Syndrome). Cornelia de lange syndrome (CDLS) is a multiple congenital anomaly syndrome.
http://www.psychnet-uk.com/dsm_iv/cornelia_de_lange_syndrome.htm

27. Brachmann-de Lange Syndrome (www.whonamedit.com)
Brachmannde lange syndrome Amstelodamensis typus degenerativus, Amsterdam degeneration type Lange, Amsterdam dwarf, congenital (embryological) malformation
http://www.whonamedit.com/synd.cfm/1080.html

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Brachmann-de Lange syndrome Also known as:
Cornelia de Lange's syndrome
Brachmann-Cornelia de Lange syndrome de Lange’s syndrome Associated persons: Winfried Robert Clemens Brachmann Cornelia Catharina de Lange Description: This condition is described sometimes as one syndrome, sometimes as two. It is here entered as one entity. A rare form of oligophrenia comprising microcephaly with severe mental retardation, short stature, and characteristic facies. Craniofacial features consist of a clown-like appearance with large, low and curly eyelashes, micrognathia, thin lips and downturned upper lip (carp mouth), cleft lip and palate, optic atrophy, an upturned nose, and hirsutism. The most striking feature of the syndrome is that all the children look alike, like brothers and sisters. Often severe dysplasia of extremities. There is a lobster-claw deformity of the hand, small hands and feet with small and tapered digits, syndactyly between the second and third toes, proximal insertion of the thumb, short and curved fifth finger, phocomelia, and oligodactyly. various other malformations. Cutis marmorata, circumoral cyanosis, generalized hypertrichosis, hypoplastic nipples and umbilicus, and simian creases are the principal dermatological features. Low birth weight after full-term pregnancy and a low-pitched growling cry are the early symptoms. The majority of those affected have diminished sucking and swallowing capacity, failure to thrive, predisposition to respiratory tract infections, and frequent vomiting with aspiration pneumonia. Mental retardation is usually severe. Most patients die before the age of 6 years. The aetiology is unknown.

28. NEWS FLASH
THE CORNELIA de lange syndrome GENE IS IDENTIFIED A team of researchers at The Children s Hospital of Philadelphia (CHOP) and Newcastle University in the UK
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THE CORNELIA DE LANGE SYNDROME GENE IS IDENTIFIED

A team of researchers at The Children's Hospital of Philadelphia (CHOP) and Newcastle University in the UK have ended a 15 year search for the gene that causes Cornelia de Lange Syndrome. The findings, reported in Nature Genetics, identified a gene on chromosome 5.
Members of the CdLS Association of Australasia are elated at these findings for various reasons:
• It will provide accurate diagnosis
• It will provide genetic testing for other family members, particularly siblings
• It will provide accurate information and counselling resources for future pregnancies • It will enable care providers to understand the diagnosis of CdLS, improve existing therapies, and design new medical therapies • It will provide a greater understand the role the gene plays in development For more information visit www.cdlsworld.org

29. OMIM - CORNELIA DE LANGE SYNDROME 1; CDL1

http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122470

30. Entrez PubMed
Cornelia de lange syndrome associated with cecal volvulus report of a case. Masumoto K, Izaki T, Arima T. Department of Pediatric
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

31. Welcome To The UC Davis Children's Hospital Cleft & Craniofacial Program
Cornelia de lange syndrome is also sometimes referred to as CdLs for short or Brachmande lange syndrome. What does Cornelia de
http://www.ucdmc.ucdavis.edu/cleft/craniofacial/guide/about/corneliadelange.html
Home Craniofacial Anomalies About Craniofacial Anomalies Team Approach to Care ... Scheduling an Appointment Cornelia de Lange Syndrome is also sometimes referred to as CdLs for short or Brachman-de Lange Syndrome. What does Cornelia de Lange Syndrome mean for a child?
Cornelia de Lange Syndrome is diagnosed by clinical features. Children with this Syndrome often have long eyelashes, bushy eyebrows and synophrys (joined eyebrows). Their hairline may be lower than other family members, and they may have more body hair. These features are often less obvious in males after puberty. Children are often shorter than others in the family. None of these features may cause a problem for the person concerned; they are just clues for a diagnosis.
Cornelia de Lange Syndrome, however, is associated with other features that can cause problems. Children with Cornelia de Lange Syndrome do not necessarily have all of these problems and the severity of the problems does vary. Children with CdLs may have gastrointestinal tract difficulties. These can include vomiting, intermittent poor appetite, constipation, diarrhea or gaseous distention. The gastrointestinal symptoms range from mild to severe.
Most children with this Syndrome will have learning problems, although there have been children with CdLs reported with normal or only slightly below normal intelligence.

32. Bbc.co.uk - Health - Illnesses And Conditions Cornelia De Lange Syndrome
A guide to Cornelia de lange syndrome, facts about the condition and where to go for support. Cornelia de lange syndrome By Dr Trisha Macnair.
http://www.bbc.co.uk/health/conditions/cornelia.shtml
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Cornelia de Lange Syndrome By Dr Trisha Macnair This syndrome encompasses characteristic physical features, developmental abnormalities and learning difficulty. Children with the syndrome are small at birth and remain small for their age. They are slow learners, although this symptom varies from mild to severe. Most will have limb abnormalities that range from small arms to complete absence of the forearms. Facial features include hirsutism (hairiness), thin eyebrows that often meet in the middle, long eyelashes, low set ears, widely spaced teeth, a short upturned nose and down-turned lips. Fits (seizures) are a common problem. 1 in 40,000 babies are born with the condition - about 38 each year in the UK. Cause is unknown - a genetic abnormality is suspected but has not yet been identified. Incidence is sporadic. It is likely that if a gene is involved it is a rare and random mutation. This mutant gene is almost never passed on to the next generation, as affected individuals seldom have children of their own - although there have been rare instances in which mildly affected individuals have also had children with the syndrome.

33. Cornelia De Lange Syndrome
Cornelia de lange syndrome Important It is possible that the main title of the report Cornelia de lange syndrome is not the name you expected.
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Health Topics Symptoms ... For a Complete Report Cornelia de Lange Syndrome Important It is possible that the main title of the report Cornelia de Lange Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms
  • BDLS Brachmann-de Lange Syndrome CdLS de Lange Syndrome
Disorder Subdivisions
  • None
General Discussion In most individuals with the disorder, Cornelia de Lange syndrome appears to occur randomly for unknown reasons (sporadic). However, there have been some familial cases, suggesting autosomal dominant inheritance. According to investigators, the disorder may be caused by changes (mutations) of a gene or genes on the long arm (q) of chromosome 3 (3q26.3). Resources Children's Craniofacial Association 13140 Coit Road Dallas, TX 75240

34. Cornelia De Lange Syndrome Information Diseases Database
Cornelia de lange syndrome,de lange syndrome,Amsterdam dwarfism,BrachmannCornelia de lange syndrome, Disease Database Information.
http://www.diseasesdatabase.com/ddb29651.htm
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35. Bruch-de Lange Syndrome Information Diseases Database
Bruchde lange syndrome may cause or Medical information linksBruch-de lange syndrome specific sites. Medical dictionary, library
http://www.diseasesdatabase.com/ddb33009.htm
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Bruch-de Lange syndrome Bruch-de Lange syndrome: Definition(s) via UMLS Code translations and terms via UMLS Bruch-de Lange syndrome: specific sites Send Bruch-de Lange syndrome to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these:
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36. Gene Discovered For Cornelia De Lange Syndrome, A Disabling Genetic Disease
Cornelia de lange syndrome Medical Dictionary definitions of MedicineNet Home MedTerms medical dictionary AZ List Cornelia de lange syndrome. In familial de lange syndrome, a gene on chromosome 5 is mutated.
http://www.newshub.com/cgibin/rd.cgi?11956972

37. Brachmann-de Lange Syndrome - Medical Dictionary Definitions Of Popular Medical
MedicineNet Home MedTerms medical dictionary AZ List Brachmannde lange syndrome. Advanced Search.
http://www.medterms.com/script/main/art.asp?articlekey=13396

38. Cornelia De Lange Syndrome - Description And Links
What is Cornelia de lange syndrome (CdLS)? Further information is available from The Cornelia de lange syndrome Foundation, Inc.
http://www.isn.net/~jypsy/corndl.htm
What is Cornelia de Lange Syndrome (CdLS)? "Syndrome" is a medical term for a condition in which there is a collection of signs (observable body changes) and symptoms (problems related by the patient) recognizable by a doctor's exam. Although individuals with the syndrome may not have all of the signs and symptoms, they will have enough to be considered "diagnostic." Individual signs and symptoms may be seen in people without the syndrome. In 1933, Dr. Cornelia de Lange, a Dutch pediatrician, described two children with similar features. She is now generally credited with describing the collection of symptoms comprising the syndrome that bears her name. The syndrome is sometimes referred to as Brachmann-de Lange Syndrome, after Dr. W. Brachmann who described a similar patient in 1916. How can CdLS be recognized? As with other syndromes, individuals with CdLS strongly resemble one another. Common characteristics include: low birthweight (usually, but not always, under five pounds), delayed 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.

39. TheFetus.net - Cornelia De Lange Syndrome -Philippe Jeanty, MD, PhD
Cornelia de lange syndrome. Philippe Jeanty, MD, PhD. Synonyms Brachmannde lange syndrome; Brachmann made the first description in 19161.
http://www.thefetus.net/page.php?id=412

40. Cornelia De Lange Syndrome Forum
Cornelia de lange syndrome Forum. anna on May 11, 2004 adoption. sarah on May 13, 2004. Cornelia de lange syndrome Gene is identified. Anonymous on May 17, 2004.
http://www.network54.com/Forum/goto?forumid=8137

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