81. Infant Teaches Christmas Spirit Gavin was tentatively diagnosed (there is no conclusive test) at five weeks old with costello syndrome, an extremely rare disease that has only been diagnosed http://www.fuquay-varinaindependent.com/news/2003122400551.html

Fuquay-Varina Independent, Gavin's first photo with Santa and his brother, Dylan, and sister, Taylor. Infant teaches Christmas spirit By Kirk Nuss staff writer kirkenuss@hotmail.com December 24, 2003 Many of us may look under the tree this holiday season for the biggest gift. After all, we may assume, the bigger the better. For Denise and David Bailey and their children Dylan, 7, and Taylor, 4, they have learned this holiday season that "Good things come in small packages." Denise and David's youngest child, Gavin, who will be seven months old this Dec. 28, currently weighs 12 pounds 6 ounces, well under the average weight for his age of 17 pounds. In fact, he is more the size of an average two month old. He did not start out so small-weighing 8 pounds at his birth on May 28, 2003. Gavin experienced some difficulty eating as a newborn but is eating fine now. But due to a congenital heart defect, he is diverting every calorie to maintain his heart. He has gone through four surgeries since July and will need one more within the next few weeks. His heart is working overtime to pump due to holes in the heart, and surgeons are not sure how best to repair them at this point. Gavin was tentatively diagnosed (there is no conclusive test) at five weeks old with Costello Syndrome, an extremely rare disease that has only been diagnosed in 150 people worldwide-of which only 26 cases are not disputed. The chances of being born with the syndrome are only one in 60 million.

82. GeneCard For CTLO IMPORTANT NOTE This gene symbol CTLO( costello syndrome ) is extracted from the *** LocusLink Database *** and is NOT approved by the HUGO Gene http://genecards.bcgsc.ca/cgi-bin/carddisp?CTLO

83. Institut Für Humangenetik E., Tímár, L., and Solyom, E. Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with costello syndrome. http://ihg.uke.uni-hamburg.de/publikationen.de.php?forscher=kk

84. Online And Offline Support: C costello syndrome. International costello syndrome Support Group People served Parents of children with costello syndrome; Services http://www.widesmiles.org/support/c.html

C CardioFacioCutaneous Syndrome CardioFacioCutaneous Support Network People served: Individuals and their families dealing with CardioFacioCutaneous Services provided: Information and referral, support services, registry, and printed materials Address: 157 Alder Avenue, McKee City NJ 08232 Phone number: (609) 646-5606 CHARGE Syndrome CHARGE Syndrome Foundation People served: Individuals and families dealing with CHARGE Syndrome Services provided: Information and referral and support 2004 Parkade Boulevard, Columbia MO 65202-3121 Phone numbers: 1-800-442-7604 (Families Only) or (573) 499-4694 Contact person: Marion Norbury Email address: marion@chargesyndrome.org or mnorbury@coin.org Website: http://www.chargesyndrome.org/ Minnow's CHARGE WebPage People Served: Individuals and families dealing with CHARGE Syndrome Services provided: Listserv, online and offline resources, realtime chats, and photo gallery Contact person: Casey Fisher Email address: charge@saber.net Website: http://www.geocities.com/Heartland/1220/ Chromosome Deletions, Chromosome Deletions, Additions, Inversions, Translocations and Rings Chromosome Deletion Outreach People served: Families dealing with chromosomal abnormalities Services provided: Support and information, chats, email support group

85. Taipei Times - Archives Taiwan has first case of very rare costello syndrome. Most cases of costello syndrome are isolated with no other family members affected. http://www.taipeitimes.com/News/local/archives/2000/06/08/39180

Thu, Jun 08, 2000 News Editorials e-Industry e-Service ... Classified 109746656 visits Front Page * MJIB, Chen lock horns over role * KMT reform to bar criminals, boost minorities Local News ... Computex 2004 Back Issue Full List TaipeiTimes Subscribe Employment FAQ About Us Contact Us Best View in Mozilla Search Advanced Search Most Read Story Most Viewed Photo Print Mail Taiwan has first case of very rare Costello Syndrome STAFF WRITER Thursday, Jun 08, 2000,Page 2 Advertising The first domestic case of Costello Syndrome, a rare disease which excessively stunts a child's growth and can cause mental retardation, was reported at Changkeng children's hospital yesterday. According to doctor Hou Chia-wei ( «J®aÞ³ ), the girl was first brought to hospital for stunted development, weighing only 7kg at the age of two. The young girl has a broad flat nose, curly hair and dark skin. Hou said more examinations are needed to determine if the girl has suffered mental retardation, as she can not speak. The mother of the girl said she has suffered prejudice and was mocked as a result of her appearance.

86. J Med Genet -- FEINGOLD 36 (7): 582 costello syndrome and rhabdomyosarcoma. EDITOR Kerr et al 1 reported two children with costello syndrome who also had embryonal rhabdomyosarcomas. http://www.jmedgenet.com/cgi/content/full/36/7/582

HOME HELP FEEDBACK SUBSCRIPTIONS ... Email this link to a friend eLetters: Submit a response to this article Similar articles found in: J Med Genet PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: FEINGOLD, M. Alert me when: new articles cite this article Download to Citation Manager Collections under which this article appears: Other Oncology Genetics J Med Genet 582-583 ( July ) Letters to the editor Costello syndrome and rhabdomyosarcoma E DITOR Kerr et al reported two children with Costello syndrome who also had embryonal rhabdomyosarcomas. I report a 14 year boy with Costello syndrome and an alveolar rhabdomyosarcoma. The baby was born after 35 weeks gestation but weighed 3544 g. Polyhydramnios was present. At birth the infant appeared to be somewhat dysmorphic, was oedematous, and had low set ears. He required a respirator for five days. His oral intake was poor and at the age of 2 weeks he was admitted to hospital because of failure to thrive. At the age of 6 months, a diagnosis of alveolar rhabdomyosarcoma of the right foot was made. Treatment consisted

87. Forum 2004 Replies 0. costello syndrome Schweiz Posted By costello syndrome Deutsche Spr, Mon Apr 26 042000 MDT 2004 Replies 1. My 6 http://forum.cjb.net:81/cgi-bin/forum.cgi?forum=costellokids

88. GREENSEEK See also Health Conditions and Diseases Rare Disorders (110). » Costello Kids Official site of the International costello syndrome Support Group. http://www.greenseek.de/internet/index.php/Health/Conditions_and_Diseases/Geneti

SEITE ANMELDEN NEUZUGÄNGE IM KATALOG FORUM UND COMMUNITY WETTERBERICHTE ... WEBDESIGN-VORLAGEN an abmelden im Katalog deutschem Web gesamten Web internationaler Katalog KATALOG Health See also: Health: Conditions and Diseases: Rare Disorders Costello Kids - Official site of the International Costello Syndrome Support Group. Includes medical information, photographs and videos, therapy ideas, news, and links. Online Mendelian Inheritance in Man: Costello Syndrome - References, gene map, and clinical synopsis. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The content of this directory is based on the Open Directory Powered by GREENSEEK

89. Costellon Oireyhtymä (FCS) Faciocutaneoskeletal syndrome Kasvo, iho- ja luusto-oireiden yhtymä FCS olleet satunnaisen mutaation aiheuttamia Uusiseelantilainen costello kuvasi oireiston v http://www.saunalahti.fi/kup/syndroma/costello.htm

Kehitysvammahuollon tietopankki Kehitysviive, karkeahkot kasvonpiirteet, nenän papillooma-kasvain, käsien ja jalkojen ihon velttous Costellon oireyhtymä Faciocutaneoskeletal Syndrome Kasvo-, iho- ja luusto-oireiden yhtymä FCS-oireyhtymä Costellon oireyhtymää luonnehtii kasvu- ja psyykkisen kehityksen viivästyminen, karkeahkot kasvonpiirteet, nenän papillooma-kasvain, käsien ja jalkojen ihon velttous sekä muut epämuodostumat. Vammautuneen pää on isokokoinen ja fontanellit suuret tai viivästyneesti sulkeutuneet. Korvat ovat matalalle asettuneet ja korvalehdet ovat laajat. Silmien luomiraot ovat alaspäin vinot ja karsastus on tavanomaista, samoin silmäkulmien laskostuminen ja matalanenäisyys. Muita piirteitä voivat olla leveä suu, paksut huulet, suuri kieli, korkea suulaki, hammaskiilteen kehityshäiriö, lyhyt kaula, tynnyrimäinen rintakehä, vatsatyrä, kämmenien ja ja jalanpohjien sarveistuminen, kämmenen puoleiset luomet, lyhyet ja litteät sormet, kyynärluiden vinous, jalkojen virheasennot, syvät kämmenien ja jalanpohjien ihouurteet. Lisäksi Akilles-jänne saattaa olla tiukka, iho ylipigmentoitunut, taipeiden orvaskeden paksuuntumat tummat, käsissä ja jaloissa voi esiintyä ihopuutoksia, ohuet kynnet ovat syvälle asettuneet. Edelleen kasvojen yläosan karvaisuus sekä kiharainen, harva ja lyhyt tukka voivat kuulua oireistoon. Hermojärjestelmän ongelmia ovat aivojen surkastuminen ja hydrokefalia . Sydänlihassairaus ja kohtauksittainen eteisvärinä kuuluvat niinikään oireisiin, samoin piilokivekset.

90. A. F. S. Costello - Redirect By Ulimit.com syndrome de costello, costello, maladie, orpheline, génétique, syndrome, afscostello, génome, gènes, association, contact, handicap, maladies orphelines http://www.afscostello.fr.st/

syndrome de costello, Costello, maladie, orpheline, génétique, syndrome, afscostello, génome, gènes, association, contact, handicap, maladies orphelines, maladie orpheline, maladies rares, maladie rare Association Française du Syndrome de Costello This document is designed to be viewed using Frame features. If you are seeing this message, please consider upgrading to a frames-compatible browser such as Click here for http://www.afscostello.fr.st Ulimit.com is a free URL redirection service. If you have a homepage with a long or difficult URL you can get a permanent short URL totally free from Ulimit.com. We have several cool names to choose from: fr.fm to linux-fan.com (click on the pulldown menu below to see the complete list and make your selection). You will also get a free matching Email address with your new identity. Redirect by Ulimit.com

91. Electricbrain Home: Index: Health: Conditions And Diseases: Genetic Disorders: C Health Conditions and Diseases Genetic Disorders costello syndrome News at 0422 on May 15, 2004 Random quote Little http://www.electricbrain.com/index/Health/Conditions_and_Diseases/Genetic_Disord

electricbrain Index Health Conditions and Diseases ... Genetic Disorders : Costello Syndrome home index write privacy ... cache Quote of the Minute... Bernard Shaw is an excellent man; he has not an enemy in the world, and none of his friends like him either. Oscar Wilde Find someone: Old Friends New Friends Lost Love New Love ... privacy

92. Assoc. Fr. Du Syndrome De Costello Translate this page Sigle. Intitulé. Association française du syndrome de costello. Activités. Connaissance clinique et scientifique de la maladie. Adresse. 48. rue. du Chouiney. 33170. http://www.fraternitaire.com/Association/AFSC.htm

Coordonnées extraites de l'annuaire des associations Sigle Intitulé Association française du syndrome de Costello Activités Connaissance clinique et scientifique de la maladie Adresse rue du Chouiney Gradignan France Tél Fax Internet Retour à la page précédente

93. COSTELLO (1977) - NOONAN-LIKE SYNDROME WITH NASAL PAPILLOMATA Features Listed For costello (1977) NOONAN-LIKE syndrome WITH NASAL PAPILLOMATA. McKusick 218040. Abnormal/deep plantar creases; http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?2008

94. Gimenei >> Health >> Conditions_and_Diseases >> Genetic_Disorders >> Costello_Sy Gimenei.com, Search for Scope All Words, Results per page 10. Request Timeout 2, http://www.gimenei.com/directory/top/Health/Conditions_and_Diseases/Genetic_Diso

Search for: Scope: All Words Any Word Phrase Results per page: Request Timeout: Search Depth: Gimenei Health Conditions and Diseases Genetic Disorders Costello Syndrome Kitchen:

95. æ“V«Ž¾Š³‚̃Tƒ|[ƒgƒOƒ‹[ƒvî•ñ The summary for this Japanese page contains characters that cannot be correctly displayed in this language/character set. http://www.mirai.ne.jp/~mizuno/support-j.htm

i‰E—ñ‚͍‘ŠO‚̃TƒCƒgAÅ‰E—ñ‚͐ê–å‰ÆŒü‚¯ƒTƒCƒgj@‹Œ”Å‚Í w•ŸŽƒ ‚ƏáŠQŽÒŽx‰‡î•ñ‚Ì‘–ÚŽŸx MUMS National Parent-to-Parent Network u‚³‚ë‚ñvŠ³ŽÒáŠQŽÒ ’c‘́^Ž©•ƒOƒ‹[ƒvƒKƒCƒh Family Village “ï•aî•ñƒZƒ“ƒ^[ National Organization for Rare Disorders (NORD) ... Special Child Magazine õF‘ÌŽ¾Š³ ƒ_ƒEƒ“ÇŒóŒQ National Down syndrome Congress ƒOƒ‹[ƒv‚½‚ñ‚Û‚Û ƒGƒ“ƒWƒFƒ‹ @iˆ¤’mŒ§j The Down Syndrome Reseach Foundation ƒsƒ ƒA @iŠò •ŒŒ§j ‚S”ԐõF‘Ì 4p- Support Gruop (Wolf-Hirschhorn Syndrome) Cri Du Chat Support Group of Australia i“Œ‹žˆã‰È‘åŠwˆâ“`Œ¤‹†Žºj Cri-du-Chat Syndrome Support Group 5p- Society ‚W”ԐõF‘Ì Trisomy 8 ‚X”ԐõF‘́@ Chromosome 9p Netwo‚’‚‹ Trisomy 9 International Parent Support ‚P‚O”ԐõF‘Ì Distal trisomy 10q families ‚P‚P”ԐõF‘Ì 11q Network i‰¢Bj@ The Jacobsen syndrome reference database 11q Net i•Ä‘j Int'l 11;22 translocation Network SOFT :Support Organization for Trisomy 18, 13 and Related Disorders ‚P‚U”ԐõF‘Ì Disorders of Chromosome 16 Foundation ‚P‚W”ԐõF‘Ì The Chromosome 18 Registry and Research Society ‚Q‚Q”ԐõF‘Ì ‚Q‚Q‚‘‚P‚PD‚QŒ‡Ž¸ÇŒóŒQF‚Q‚QHeart Club Parent Support Group for Chromosome 22 related disorders Chromosome 22 Central Ring 22 ... Anneau 22 ƒ^[ƒi[ÇŒóŒQAƒgƒŠƒvƒ‹XÇŒóŒQAX‰ßèÇŒóŒQ ƒgƒŠƒvƒ‹X—« iTriple X female) Tetra/Pentasomy X Support Group ƒNƒ‰ƒCƒ“ƒtƒFƒ‹ƒ^[ÇŒóŒQ Kleinfelter Suppot Group Understanding KFS @ E ‚`‚`‚j‚r‚h‚r ¬‡«‘BˆÙŒ`¬Ç Mixed gonadal dysgenesis support group ‚»‚Ì‘¼‚̐õF‘ÌŽ¾Š³A‹H­õF‘Ì‹NˆöŽ¾Š³ CDOF Chromosome Deletion Outreach UNIQUE : Rare chromosome disorders

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 5     81-95 of 95    Back | 1  | 2  | 3  | 4  | 5