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         Costello Syndrome:     more detail
  1. Costello syndrome
  2. Costello syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Kevin, MS, CGC Sweet, 2005
  3. Costello Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
  4. Meet Krista.(Down's syndrome child): An article from: Children's Playmate by Marian Costello, 1994-07-01
  5. Clinical predictors of 30-day cardiac events in patients with acute coronary syndrome at a community hospital.(Original Article): An article from: Southern Medical Journal by George M. Tadros, Timothy R. McConnell, et all 2003-11-01
  6. Carbohydrate intolerance: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Karen, R.N. Ericson, Angela Costello, 2006
  7. Anomalies and Curiosities of Medicine by George M. Gould, 2010-08-02
  8. Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-08-02
  9. Anomalies and Curiosities of Medicine by George M. Gould, 2010-08-02
  10. Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-06-20
  11. Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-09-20
  12. Anomalies And Curiosities Of Medicine- George M. Gould, A.M., M.D. by A.M., M.D. George M. Gould, 2010-02-17

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 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

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

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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
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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
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Health Conditions and Diseases ... Genetic Disorders : Costello Syndrome home index write privacy ... cache
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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
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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
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w•ŸŽƒ ‚ƏáŠQŽÒŽx‰‡î•ñ‚Ì‘–ÚŽŸx
MUMS National Parent-to-Parent Network
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National Organization for Rare Disorders (NORD) ... Special Child Magazine
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National Down syndrome Congress

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ƒGƒ“ƒWƒFƒ‹ @iˆ¤’mŒ§j The Down Syndrome Reseach Foundation
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‚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

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