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         Cri Du Chat Syndrome:     more detail
  1. Cri du chat syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Judith Sims, Holly, M.S. Ishmael, 2006
  2. Cri-Du-Chat Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
  3. Gale Encyclopedia of Medicine: Cri du chat syndrome by Holly Ann Ishmael M.S., 2002-01-01
  4. Using Parent-Delivered Graduated Guidance to Teach Functional Living Skills to a Child with Cri du Chat Syndrome.: An article from: Education & Treatment of Children by Michael Denny, Nancy Marchand-Martella, et all 2000-11-01
  5. Cri Du Chat Syndrome: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Holly, M.S. Ishmael, Rebecca, PhD Frey, 2006
  6. Cri du chat syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Holly, MS, CGC Ishmael, 2005

41. Cri Du Chat Syndrome 5p- Information Diseases Database
cri du chat syndrome 5p,5p partial monosomy syndrome,Cat s cry syndrome, Disease Database Information.
http://www.diseasesdatabase.com/ddb29133.htm
Diseases Database Index Sponsors Contact ... Previous Page
Cri du chat syndrome 5p- Information
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3 synonyms or equivalents were found. Cri du chat syndrome 5p-
aka/or
5p partial monosomy syndrome
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Cat's cry syndrome Cri du chat syndrome 5p-: Definition(s) via UMLS Code translations and terms via UMLS Cri du chat syndrome 5p-: specific sites Send Cri du chat syndrome 5p- to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these:
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42. Cri Du Chat
Collins, MS Ross; Cornish, K. A survey of the prevalence of stereotypy, selfinjury and aggression in children and young adults with cri du chat syndrome.
http://www.genesoc.com/counseling/Outlines/criduchat.htm
Resources for Genetic Counselors site updated May 10, 2004 outlines links search Cri-du-chat syndrome (deletion 5p)
Contracting
  • Introduction Ask about what their main concerns are Explain that we will update medical and developmental history since her last visit to genetics Doctor will perform physical examination We will discuss your concerns and any recommendations we have
Interim History Follow form, but specifically ask about list of potential health problems located below
Overview
  • Cri du chat is a syndrome that is associated with a deletion of the short arm of chromosome 5 French for “cat’s cry” incidence is 1:50,000 (Van Buggenout et al, 2000 ) may be as high as 1:20,000 (OMIM)
Characteristic features
  • usually suspected at birth based on characteristic monochromatic, high-pitched cry poor suck, vomiting, failure to thrive, respiratory distress and jaundice present in 60-92% microcephaly round face hypertelorism epicanthal folds down-slanting palpebral fissures low-set ears micrognathia psychomotor retardation high arched palate
*** as individuals with 5p deletion get older change of phenotype is noted and it is less striking and harder to diagnose (face lengthens, face becomes “coarse”, prominent supra-orbital ridges, deep-set eyes, hypoplastic nasal bridge, severe dental malocclusion, relatively large mouth, and full lower lip)

43. Cri-du-Chat (5p-)Syndrome
site http//www.vicnet.net.au/~criduch/ cri du chat syndrome Support Group, United Kingdom; 5p Family Support Services, Canada;
http://www.kumc.edu/gec/support/cri-du-c.html
Cri-du-Chat (5p-)
5p- Society (Cri-du-Chat)
11609 Oakmont Overland Park, KS 66210 Phone: (913) 469-8900 E-mail: fivepminus@aol.com Web Site: http://www.fivepminus.org/
Cri Du Chat Support Group of Australia
5 Connal Drive, Frankston, VIC 3199 E-mail: maggiecdc@bigfoot.com Web site: http://www.vicnet.net.au/~criduch/
Also See:

44. CRI DU CHAT SYNDROME !
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cri du chat syndrome Both girl's spied the bosses feeble attempt to hide a 10" hard on and looked at each with a glint in their eye cri du chat pictures.
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45. Neurological Disorders, Chromosomal, Cri Du Chat Syndrome
More cri du chat syndrome Categories » Submit Your Site to the cri du chat syndrome category. Submit Your Site to the cri du chat syndrome category.
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46. Disease - Cri Du Chat Syndrome - Hartford, Connecticut , Saint Francis Care
Disease cri du chat syndrome - courtesy of Saint Francis Care of Hartford, Connecticut, contemporary medicine with major clinical concentrations in heart
http://www.saintfranciscare.com/11766.cfm
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Disease - Cri du chat syndrome
Definition: Cri du chat syndrome is a group of symptoms that result from missing a piece of chromosome Alternative Names: Chromosome 5p deletion syndrome; 5p minus syndrome; Cat cry syndrome Causes And Risk: The cri du chat syndrome is caused by the deletion of information on chromosome 5. It is likely that multiple genes on chromosome 5 are deleted. One deleted gene, called TERT (telomerase reverse transcriptase) is involved in control of cell growth, and may play a role in how some of the features of cri cu chat develop. The cause of this rare chromosomal deletion is not known, but it is expected that the majority of cases are due to spontaneous loss of a piece of chromosome 5 during development of an egg or sperm. A minority of cases result from one parent carrying a rearrangement of chromosome 5 called a translocation. Between 1 in 20,000 and 1 in 50,000 babies are affected. This disease may account for up to 1% of individuals with severe mental retardation. Infants with cri du chat syndrome commonly have a distinctive cat-like cry. They also have an extensive grouping of abnormalities with severe mental retardation being the most important.

47. Cri Du Chat Syndrome
Other characters, cri du chat syndrome,. Print this article, see chromosome 5 deletion. HC. The Encyclopaedia of Medical Imaging Volume VII.
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/CRI DU CHAT SYND
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Cri du chat syndrome, see chromosome 5 deletion
HC
The Encyclopaedia of Medical Imaging Volume VII
Contacts
GE Healthcare Making Waves

48. Cri Du Chat Syndrome
N, O, P, Q, R, S, T, U, V, W, X, Y, Z, Other characters, cri du chat syndrome,. Print this article, syndrome resulting from a chromosomal aberration consiting of 5p deletion.
http://www.amershamhealth.com/medcyclopaedia/Volume V 2/CRI DU CHAT SYNDROME.asp
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Cri du chat syndrome, syndrome resulting from a chromosomal aberration consiting of 5p- deletion. About 20% of these patients have congenital heart disease of which the most frequent lesions are ventricular septal defect atrial septal defect patent ductus arteriosus or pulmonary artery stenosis . The major features of this syndrome are a cry reminescent of a cat, microcephaly and mental retardation.
CBH
The Encyclopaedia of Medical Imaging Volume V:2 Contacts GE Healthcare Making Waves

49. What Is Cri Du Chat Syndrome
What is cri du chat syndrome? Cri du Chat (KREE doo SHAH) Syndrome is a chromosomal disorder where the short arm of the fifth chromosome
http://www.thehutchpage.com/aboutcriduchat.htm
What is Cri du Chat Syndrome? Cri du Chat (KREE doo SHAH) Syndrome is a chromosomal disorder where the short arm of the fifth chromosome is lost from the first cell of life. All of our genes are attached to chromosomes. So when a piece of a chromosome is lost, so is a piece of the genetic code that makes us who we are. In approximately 90 percent of cases, including Vincent's, both parents are chromosomally normal and the deletion occurs spontaneously for reasons that geneticists cannot yet explain. The syndrome is rare. Estimates of its occurrence range from one in 30,000 to one in 50,000 live births. Undoubtedly this accounts for the relative paucity of information on Cri du Chat, as compared to more commonly known chromosomal disorders such as Down's Syndrome. Like most chromosomal disorders, Cri du Chat presents an array of developmental challenges intellectual as well as physical. Mental retardation ranges from mild to severe, with most cases falling into the moderate range. Communication is the most significant challenge for persons with this syndrome. Some form of sign language is a must. Physical development is impaired primarily by low muscle tone, which underscores the importance of early intervention in the form of physical therapy. It is considered exceptional for a child with this syndrome to walk before 3 years old. Some people with the syndrome are never able to walk at all.

50. Disease Directory : Neurological Disorders : Chromosomal : Cri Du Chat Syndrome
Diseases Neurological Disorders Chromosomal cri du chat syndrome. Cridu-chat Support Group of Australia - Comprehensive information
http://www.diseasedirectory.net/Neurological_Disorders/Chromosomal/Cri_du_Chat_S
Wednesday, June 02, 2004 Neurological Disorders Chromosomal
Cornelia De Lange Syndrome

Cri du Chat Syndrome
... Chromosomal : Cri du Chat Syndrome

51. Library Pages 1 To 5
5p deletion (cri du chat syndrome) Clinical and molecular characterization of 80 patients with 5p deletion genotypephenotype correlation, J. Med Genetics
http://www.chromodisorder.org/sytrix/card_list.php3?dbid=78&id=155

52. Short Description Of Cell Lines. Pathology: Cri Du Chat Syndrome #123450
Version 4.200205, Short description of cell lines. Pathology cri du chat syndrome 123450 OMIM record. By selecting the cell line
http://www.biotech.ist.unige.it/cldb/pat170.html
Version
Short description of cell lines.
Pathology: cri du chat syndrome
OMIM record
By selecting the cell line name , you will receive the detailed description of the cell line
By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines
You can search any term of the list by using the 'Find' utility of your browser
human, Caucasian
lymphocyte GGB
C-C95
...
By Beatrice...

53. Cri Du Chat
Complete description of the cell line that you requested. Cri du Chat (human, Caucasian, skin, fibroblast, cri du chat syndrome 123450 (OMIM record) ).
http://www.biotech.ist.unige.it/cldb/cl910.html
Version
Complete description of the cell line that you requested.
Cri du Chat ( human, Caucasian skin, fibroblast cri du chat syndrome (OMIM record)
ECACC 90102533
Morphology: Fibroblast
Human Caucasian skin deletion in chromosome 5
Depositor: Obtained from ATCC, USA
No restrictions. Patent: None Specified By Depositor
Properties: Applications: Chromosome studies
Available in the following LABORATORY
  • (ECACC, Salisbury, Wiltshire)
    McCoy's 5a + 2mM Glutamine + 20% Fetal Bovine Serum (FBS). Split confluent cultures 1:3 i.e. seeding at 5x10,000 cells/cm2 using 0.25% trypsin; 5% CO2; 37C. Cells should not be centrifuged. Passages: 17 Karyotype: 2n = 46, diploid
    Hazard: CX
    Derived from the skin of an adult female Caucasian with Cri du Chat syndrome. The cells have a deletion in chromosome 5 and have a finite lifespan; up to 35 population doublings expected. Further information Research council deposit: No Price_code: C
Availability in cell line catalogues ATCC CCL 90; Bibliographic references:
  • Cytogenetics 1966;5:137
By Beatrice...

54. :: Ez2Find :: Cri Du Chat Syndrome
Guide cri du chat syndrome, Nickname, Chat mode Avatar Chat There are currently users online. Metasearch ICQ. Guides, cri du chat syndrome.
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ez2Find Home Directory Health Conditions and Diseases ... Chromosomal : Cri du Chat Syndrome Related Categories Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Rare Disorders
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55. Neurological Disorders: Chromosomal: Cri Du Chat Syndrome
Neurological Disorders Chromosomal cri du chat syndrome. NORD cri du chat syndrome. Offers the synonyms, a general discussion and further resources.
http://www.puredirectory.com/Health/Conditions-and-Diseases/Neurological-Disorde
Neurological Disorders: Chromosomal: Cri du Chat Syndrome
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Standard Listings
Cri-du-chat Support Group of Australia
Comprehensive information on this rare genetic disorder, including its characteristics and genetic basis.
NORD: Cri du Chat Syndrome
Offers the synonyms, a general discussion and further resources.
The CaF Directory
A description of Cri du Chat Syndrome with details on the inheritance pattern and pre-natal diagnosis.
The Cri du Chat Syndrome Support Group
Information about this disease as well as a message board and a chat room.
Vincent's Home Page
Chronicling one child's journey through the medical and developmental challenges presented by Cri du Chat Syndrome.
Help build the largest human-edited directory on the web.

56. Cri Du Chat
The cri du chat syndrome. Generally / general information At Switzerland there are about 3040 children with the cri du chat syndrome.
http://mitglied.lycos.de/cdc/index-english.html
The Cri du Chat syndrome
private information from Switzerland update: 12-08-99
Generally / general information
At Switzerland there are about 30-40 children with the Cri du Chat syndrome. There is to the time at Switzerland no support group, some parents have however an active experience-exchange. We recommend the membership at the German support group. We do not know at the moment, as far this page is maintained and extended. The topic is so extensive that it is difficult to inform on private base globally. We try to translate always in english, but this will not be perfect Medical reports " development "
- the " Cri du Chat syndrome " of Stephan Berger (medical, psychosocial and educational aspects) very extensive , in german, available at the German Foerderverein.
- video about the syndrome. (16 kids across Australia and the variation.) 42 mins, PAL or NTSC, cost $AUS 45 plus shipping, contact Helen McGrath email: helliemac@ozemail.com.au
State support by the invalid-insurance (IV) - " acknowledgment of the syndrome "
The IV is regulated and therefore very different kantonal. The medical order takes place via the physician or doctor (

57. Cri Du Chat Syndrome. Iyer SL, Duraiswamy A, Kher AS, Joshi S, Bharucha BA, Kana
CASE REPORT. Year 1996 Volume 42 Issue 3 Page 868. cri du chat syndrome. cri du chat syndrome. J Postgrad Med 1996;4286-8.
http://www.jpgmonline.com/article.asp?issn=0022-3859;year=1996;volume=42;issue=3

58. Cri Du Chat Syndrome
cri du chat syndrome. Definition A group retardation. Infants with cri du chat syndrome commonly have a distinctive catlike cry. They
http://www.healthscout.com/ency/article/001593.htm
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Cri du chat syndrome
Definition: Cri du chat syndrome is a group of symptoms that result from missing a piece of chromosome number 5. The syndrome’s name is based on the infant’s cry, which is high pitched and sounds like a cat.
Alternative Names: Chromosome 5p deletion syndrome; 5p minus syndrome; Cat cry syndrome
Causes, incidence, and risk factors: The cri du chat syndrome is caused by the deletion of information on chromosome 5. It is likely that multiple genes on chromosome 5 are deleted. One deleted gene, called TERT (telomerase reverse transcriptase) is involved in control of cell growth, and may play a role in how some of the features of cri cu chat develop. The cause of this rare chromosomal deletion is not known, but it is expected that the majority of cases are due to spontaneous loss of a piece of chromosome 5 during development of an egg or sperm. A minority of cases result from one parent carrying a rearrangement of chromosome 5 called a translocation.

59. EDUCATION PLANET - 1120 Web Sites For Cri Du Chat Syndrome
cri du chat syndrome Web Sites (1 10 of 1112)
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60. Health, Conditions And Diseases, Neurological Disorders, Chromosomal: Cri Du Cha
and genetic basis. NORD cri du chat syndrome Offers the synonyms, a general discussion and further resources. The CaF Directory
http://www.combose.com/Health/Conditions_and_Diseases/Neurological_Disorders/Chr
Top Health Conditions and Diseases Neurological Disorders ... Cri du Chat Syndrome
Related links of interest: A rare chromosomal disorder that is apparent at birth, is characterized by a distinctive high, shrill, mewing, "kitten-like" cry during infancy. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The combose.com directory is based on the

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