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Cri Du Chat Syndrome: more detail

Cri du chat syndrome: An entry from Thomson Gale's Gale Encyclopedia of Children's Health: Infancy through Adolescence by Judith Sims, Holly, M.S. Ishmael, 2006
Cri-Du-Chat Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
Gale Encyclopedia of Medicine: Cri du chat syndrome by Holly Ann Ishmael M.S., 2002-01-01
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
Cri Du Chat Syndrome: An entry from Gale's Gale Encyclopedia of Medicine, 3rd ed. by Holly, M.S. Ishmael, Rebecca, PhD Frey, 2006
Cri du chat syndrome: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Holly, MS, CGC Ishmael, 2005

lists with details

Symptoms Of Cri-du-chat Syndrome - WrongDiagnosis.com
Symptoms of cridu-chat syndrome including signs, symptoms, incubation period, duration, and correct diagnosis.
http://www.wrongdiagnosis.com/c/cri_du_chat_syndrome/symptoms.htm

Extractions: Feedback General information about symptoms of Cri-du-chat syndrome: The symptom information on this page attempts to provide a list of some possible symptoms of Cri-du-chat syndrome. This symptom information has been gathered from various sources, may not be fully accurate, and may not be the full list of symptoms of Cri-du-chat syndrome. Furthermore, symptoms of Cri-du-chat syndrome may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of symptoms and whether they are indeed symptoms of Cri-du-chat syndrome. List of symptoms of Cri-du-chat syndrome: The list of symptoms mentioned in various sources for Cri-du-chat syndrome includes: More symptoms of Cri-du-chat syndrome: In addition to the above information, to get a full picture of the possible symptoms of this condition and its related conditions, it may be necessary to examine symptoms that may be caused by complications of Cri-du-chat syndrome, underlying causes of Cri-du-chat syndrome, associated conditions for Cri-du-chat syndrome, risk factors for Cri-du-chat syndrome, or other related conditions.
OMIM - CRI-DU-CHAT SYNDROME
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123450
The DRM WebWatcher: Cri-Du-Chat Syndrome
A Disability Resources Monthly guide to the best online resources about cridu-chat syndrome.
http://www.disabilityresources.org/CRI.html

Extractions: Home WebWatcher Regional Librarians ... Contact Us The DRM WebWatcher Cri-Du-Chat Syndrome Updated 3/30/2004 A B C D ... About/Hint/Link Cri-du-Chat Syndrome, also known as 5p- Syndrome (five p minus) or Cat Cry Syndrome, is a rare genetic disorder characterized at birth by a high pitched cry, low birth weight, poor muscle tone, and other anomalies. For information about Cri-Du-Chat syndrome, check these sites. 5p- Society This organization provides information about the syndrome, the organization's services, and other resources, including organizations, articles, publications and products. Cri Du Chat Support Group of Australia This Australian support group provides general information about the syndrome and the group, as well as an extensive list of related links and resources. There is also a list of international groups and contacts, a chatroom, and a messageboard. Cri-Du-Chat Syndrome A technical article with a focus on genetics from Online Mendelian Inheritance in Man (OMIM). References link to PubMed articles.
Vysis: Cri-du-Chat Syndrome LSI D5S23, D5S71 SpectrumGreen
Deletions of 5p15.2 are associated with cridu-chat syndrome. Vysis LSI D5S23, D5S721 probe detects deletions of 5p15.2. The LSI D5S23, D5S721 probe is
http://www.vysis.com/CriduChatSyndromeLSID5S23D5S71SpectrumGreen_2093.asp

Extractions: Negotiating with host Sending Data Verifying Data Receiving Data Prenatal, Postnatal and Preimplantation Genetics Chromosome Aneusomy Telomere Probes Preimplantation ... FISH Microscope Filters //HideChromo and ShowChromo moved to Specific.js 11/28/04 // NOTE: GoToChromosomePage function is located in 02/www/include/Layout/Xsl_Vysis/Javascript so // it can be used globally Cri-du-Chat Syndrome LSI D5S23, D5S71 SpectrumGreen TM
SAIDA - Cri-du-Chat Support Group
A support group for parents with children with the cridu-chat syndrome was established She has made contact with cri-du-chat syndrome support groups in
http://sunsite.wits.ac.za/saida/disorders/criduchat_society.htm

Extractions: Cri-du-Chat (5p-) syndrome occurs in about 1 in 50 000 births. The syndrome was given its name due to the distinct high pitched, cat-like cry that affected babies have because of the abnormal development of their larynx. Affected individuals have a deletion in the short arm of chromosome 5 (part of chromosome 5 is missing) so this disorder is also sometimes called 5p- syndrome. Characteristic features of this syndrome include low birth weight and delayed growth, microcephaly (small head), downward and outward slanting eyes spaced widely apart, squints, low set ears, facial asymmetry, cleft lip and palate, heart defects, renal (kidney) abnormalities, hypotonia (floppiness) and mental disability ranging from mild to severe. A support group for parents with children with the Cri-du-Chat syndrome was established in 1995. Mrs Angela Bravi is the contact person and group coordinator. She has made contact with Cri-du-Chat syndrome support groups in Australia, UK and USA. She encourages people in South Africa and the rest of the world to contact her by mail, phone or fax so she can build up the Cri-du-Chat Syndrome Support Group. Cri-du-Chat Syndrome Support Group P.O Box 640
Cri-du-chat Syndrome - Genetics Home Reference
What are the genetic changes related to cridu-chat syndrome? Can cri-du-chat cri-du-chat syndrome is a chromosomal condition related to chromosome 5.
http://ghr.nlm.nih.gov/condition=criduchatsyndrome

Extractions: Home What's New Browse Handbook ... Search Cri-du-chat syndrome On this page: Cri-du-chat (cat cry) syndrome is a chromosomal condition that results when a piece of chromosome 5 is missing. Infants with the condition often have a high-pitched cry that sounds like that of a cat. The disorder is characterized by severe mental retardation and delayed development, distinctive facial features, small head size (microcephaly), low birth weight, and weak muscle tone (hypotonia) in infancy. This condition affects an estimated 1 in 20,000 to 50,000 live births. The disorder is found in people of all ethnic backgrounds and is slightly more common in females. What are the genetic changes related to cri-du-chat syndrome?
Cri-du-chat Syndrome Definition
cridu-chat syndrome. Definition. Search for. Glossary - word, Glossary - def, Textbooks, Protocols, Images, Tools, Forum, PubMed, Links, Press Releases
http://www.biochem.northwestern.edu/holmgren/Glossary/Definitions/Def-C/cri-du-c
Cri-du-Chat (5p-)Syndrome
cri du chat national and international support groups, clinics with genetic counselors and geneticists.
http://www.kumc.edu/gec/support/cri-du-c.html
Cri-du-Chat Syndrome: Toward A Behavioral Phenotype
cridu-chat syndrome is a relatively rare condition but represents the most common deletion syndrome in humans. At birth, the main characteristic feature is
http://www.mhaspectsofdd.com/abstracts/Vol4Num4/5.htm
Cri-du-chat.html
ABSTRACT cridu-chat syndrome is associated with a deletion of the short arm of While most display the classical phenotype of the cri-du-chat syndrome,
http://www.indiana.edu/~pietsch/cri-du-chat.html

Extractions: DEFINITION OF TERM : An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia. It is caused by a deletion of the short arm of chromosome 5 (5p-). web contact: pietsch@indiana.edu A literature search at Indiana University, Bloomington, Indiana The following MEDLINE items were compiled by SilverPlatter and are presented with their generous co-operation and permission. ( See SilverPlatter's Worldwide Library for bibliographic search information Record 1 of 22 in MEDLINE EXPRESS (R) 1998/11-1999/01 TITLE: Chromosome healing of constitutional chromosome deletions studied by microdissection. AUTHOR(S): Vermeesch-JR; Falzetti-D; Van-Buggenhout-G; Fryns-JP; Marynen-P ADDRESS OF AUTHOR: Center for Human Genetics, Flanders Interuniversity Institute for Biotechnology, University of Leuven, Leuven (Belgium). SOURCE (BIBLIOGRAPHIC CITATION): Cytogenet-Cell-Genet. 1998; 81(1): 68-72 INTERNATIONAL STANDARD SERIAL NUMBER: 0301-0171 PUBLICATION YEAR: 1998 LANGUAGE OF ARTICLE: ENGLISH COUNTRY OF PUBLICATION: SWITZERLAND MEDLINE ACCESSION NUMBER: 98358149 UPDATE CODE: 9812 Record 2 of 22 in MEDLINE EXPRESS (R) 1998/11-1999/01 TITLE: A case of monosomy 21 found to be an unbalanced de novo t(5p;21q) by fluorescence in situ hybridization. AUTHOR(S): Flaherty-L; Moloney-J; Watson-N; Robson-L; Bousfield-L; Smith-A ADDRESS OF AUTHOR: Department of Cytogenetics, New Children's Hospital, Westmead, New South Wales, Australia. SOURCE (BIBLIOGRAPHIC CITATION): J-Intellect-Disabil-Res. 1998 Jun; 42 ( Pt 3): 254-8 INTERNATIONAL STANDARD SERIAL NUMBER: 0964-2633 PUBLICATION YEAR: 1998
Cri-du-chat Syndrome: Clinical Profile And Prenatal Diagnosis. Tullu MS, Muranja
J Postgrad Med, Online version this peerreviewed periodical, a publication of the Staff Society of Seth GS Medical College and KEM Hospital, India,
http://www.jpgmonline.com/article.asp?issn=0022-3859;year=1998;volume=44;issue=4
Structural Abnormalities: Deletions (Cri Du Chat) And Duplications (Pallister Ki
cri du chat or Cat Cry syndrome is found in approximately 50 to 60 children each year born in the United States. cri du chat is caused by a deletion of
http://www.healthsystem.virginia.edu/uvahealth/peds_genetics/structur.cfm

Extractions: [ Skip Navigation ] Topics Adolescent Medicine Allergy/Asthma/Immunology Blood Disorders Burns Cancer Common Injuries/Poison Tips Craniofacial Anomalies Dermatology Diabetes/Endo/Metabolism Eye Care Genitourinary/Kidney High-Risk Newborn High-Risk Pregnancy Infectious Diseases Medical Genetics Mental Health Nervous System Disorders Normal Newborns Oral Health Orthopaedics Pediatric Surgery Respiratory Disorders Terminal Illness in Children Transplantation Search This Site Structural chromosome abnormalities occur when there is a change in the structure or components of a chromosome. The total number of chromosomes is usually normal (46 total per cell). Structural chromosome abnormalities occur when part of a chromosome is missing, a part of a chromosome is extra, or a part has switched places with another part. Ultimately, this leads to having too much or too little genetic material, which is a cause of some birth defects. Each chromosome has many segments which are usually divided into a "short arm" and a "long arm" of the chromosome. The short arm which is the upper half of the chromosome, is known as the "p arm" and the long arm, which is the lower half of the chromosome, is the "q arm."
Cri-du-Chat Syndrome Topic - Unified Search Environment
cridu-chat syndrome MSH/MH/D003410 MTHICD9/ET/758.3 COSTAR/PT/NOCODE CSP/PT/1254-8011 MSH/PM/D003410 MSH/PM/D003410 MSH/PM/D003410 MSH/PM/
http://www.use.hcn.com.au/portals/shared/subject.`Cri-du-Chat Syndrome`/home.htm

Extractions: An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia. It is caused by a deletion of the short arm of chromosome 5 (5p-). Synonyms and Source Vocabularies:
Cri Du Chat (5P) Syndrome
National network. Founded 1987. Support organization for families having a child with 5P - syndrome (aka
http://my.webmd.com/hw/raising_a_family/shc29cri.asp

Extractions: Support organization for families having a child with 5P- syndrome (aka cri du chat), genetic disorder characterized by a high-pitched cry. Dedicated to facilitating flow of information among affected families and medical professionals. Listing of families in U.S and Canada. Newsletter. Annual meeting. International chatroom (Sun. and Thurs). The above information was "verified" as correct on the date at the end of each entry. Since American Self-Help Group Clearinghouse's database is extensive but staffing is limited and information for these organizations can change, it is not possible to keep every entry in American Self-Help Group Clearinghouse database completely current and accurate. Please check with the organizations listed for the most current information. For additional information on self-help groups, please visit the American Self-Help Group Clearinghouse web site at http://www.mentalhelp.net/selfhelp
Cri-du-chat Syndrome -- Encyclopædia Britannica
cridu-chat syndrome rare congenital disorder caused by partial deletion of the short arm of chromosome 5, characterized by mental retardation,
http://www.britannica.com/eb/article-9027886

Extractions: Home Browse Newsletters Store ... Subscribe Already a member? Log in Content Related to this Topic This Article's Table of Contents cri-du-chat syndrome Print this Table of Contents Shopping Price: USD $1495 Revised, updated, and still unrivaled. The Official Scrabble Players Dictionary (Hardcover) Price: USD $15.95 The Scrabble player's bible on sale! Save 30%. Merriam-Webster's Collegiate Dictionary Price: USD $19.95 Save big on America's best-selling dictionary. Discounted 38%! More Britannica products cri-du-chat syndrome var mm = [["Jan.","January"],["Feb.","February"],["Mar.","March"],["Apr.","April"],["May","May"],["June","June"],["July","July"],["Aug.","August"],["Sept.","September"],["Oct.","October"],["Nov.","November"],["Dec.","December"]]; To cite this page: MLA style: "cri-du-chat syndrome." http://www.britannica.com/eb/article-9027886
Cri-du-Chat Syndrome
cridu-chat syndrome is a genetic disorder caused by partial deletion (loss) of part of cri-du-chat syndrome affects people of all ethnic backgrounds.
http://www.malattiemetaboliche.it/articoli/cri_du_chat_syndrome.htm

Extractions: From Mary Kugler Your Guide to Rare / Orphan Diseases Cri-du-chat syndrome is a genetic disorder caused by partial deletion loss ) of part of human Chromosome known as This chromosome error occurs during fetal development and is not inherited The estimated incidence of the syndrome in the United States is 1 in 50,000 live births Cri-du-chat syndrome affects people of all ethnic backgrounds Symptoms The syndrome gets its name (" cat' s cry ") from the characteristic cry of infants born with the disorder The infant sounds just like a mewing kitten , due to problems with the larynx and nervous system This cry identifies the syndrome About 1/3 of children lose the cry by age Other symptoms of cri-du-chat syndrome may include: Diagnosis is based on the distinctive cry and accompanying physical problems Genetic testing (FISH) can confirm the diagnosis Treatment No treatment exists for the underlying genetic disorder , so medical care is focused on the symptoms Chronic medical problems such as respiratory tract infections may occur and require treatment Heart defects may need to be corrected by surgery The child with cri-du-chat syndrome may require a gastrostomy tube for feeding To increase communication skills early intervention
HighWire -- Browse Journals - Cri-du-Chat Syndrome
Browse Journals publishing on cridu-chat syndrome, (return to Topic List page) Alphabet, , Frequency of articles in cri-du-chat syndrome
http://highwire.stanford.edu/lists/topic_dir/608683/618131/620438/620963/620971/

Extractions: Sort by: Alphabet Frequency of articles in Cri-du-Chat Syndrome Focus of journal on Cri-du-Chat Syndrome What's this? Journals focusing on Cri-du-Chat Syndrome (in order by highest focus) Genome Research info free ISSUES Human Molecular Genetics ... Nervous System Chromosomal Disorders Cri-du-Chat Syndrome Home Adv. Search For Institutions For Publishers ... partners/suppliers
Cri Du Chat, Maladie : Sites Et Documents Francophones
cri du chat . Délétion 5p - synonyme(s) et inclusion(s) cri du chat, syndrome du ; monosomie 5p Par Dr Turleau C.
http://www.chu-rouen.fr/ssf/pathol/criduchatmaladie.html

Extractions: Cri du chat, maladie Définition [MeSH Scope Note ; traduction CISMeF] : Syndrome infantile caractérisé par un cri semblable à celui des félins, un défaut de croissance, une microcéphalie, un retard mental, une quadriparésie spastiques, une micro rétrognathie, un glossoptose, un épicanthe bilatéral, un hypertelorisme, et des organes génitaux externes minuscules. Il est provoqué par une délétion du bras court du chromosome 5 (5p -).
AFCC - Association Francophone Du Syndrôme Du Cri Du Chat - CH-1485 Nuvilly
Translate this page Association traitant de la maladie du syndrôme du cri du chat - CH-Nuvilly (FR) Suisse.
http://www.criduchat.ch/
Welcome To The 5P- Society
About 5P syndrome 5P- Society s Role Homepages Annual Conference Key Resources Picture Gallery Recent Newsletter Coming Soon
http://www.fivepminus.org/

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