61. Bryan Hall The costello syndrome, Meisner RabsonMendenhall Syndrome, costello syndrome may have many of the same features (eg the dry skin and the curly hair), http://www.noonansyndrome.org/articlesinfo/Bryan Hall.htm

Home Site Map Search Contact Us ... Next Bryan Hall M.D., Chief Professor of Pediatrics "Noonan syndrome: An overview plus discussion of other similar entities" Dr Hall began by commenting that from all the parent group meetings he had attended he felt that had gained far more information than he had given out. This is because a lot of day-to-day worries and problems that we may have with our children may not otherwise be recognised by the medical profession, as parents may feel that they are not necessarily medical or not important enough to share with the doctor on a one-to-one basis. But in actual fact these are things that doctors would like to find out about, even though they can't necessarily provide any answers, and in group meetings it is possible to get very useful factual information within a very short period of time. He went on to add that sometimes he could raise a question which he thought would give a negative answer, only to find that many parents will say "my child does that" or "my child doesn't do that", and this can be extremely useful. Dr Hall then went on to show a sequence of slides showing children with Noonan Syndrome, and the following is a summary of his comments.

62. Journal Of Pediatric Orthopaedics - Abstract: Volume 23(1) January/February 2003 costello syndrome Orthopaedic Manifestations and Functional Health. Summary Sixteen individuals with costello syndrome underwent a complete history, http://www.pedorthopaedics.com/pt/re/jpedortho/abstract.00004694-200301000-00019

LWWOnline LOGIN eALERTS REGISTER ... Archive Costello Syndrome: Orthopaedic... ARTICLE LINKS: Fulltext PDF (429 K) Permissions Costello Syndrome: Orthopaedic Manifestations and Functional Health. Journal of Pediatric Orthopedics. 23(1):94-98, January/February 2003. Yassir, Walid K. M.D. *; Grottkau, Brian E. M.D. +; Goldberg, Michael J. M.D. ++ Abstract: Subscribe to RSS feed utrdc-pt02 Release 4.0

63. Journal Of Pediatric Orthopaedics - UserLogin costello syndrome Orthopaedic Manifestations and Functional Health Sixteen individuals with costello syndrome underwent a complete history, http://www.pedorthopaedics.com/pt/re/jpedortho/fulltext.00004694-200301000-00019

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64. 219200 CUTIS LAXA WITH GROWTH AND DEVELOPMENTAL DELAY Davies, SJ; Hughes, HE Cutis laxa a feature of costello syndrome. Patton, MA; Baraitser, M. Cutis laxa and the costello syndrome. J. Med. Genet. http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:219200] -e

65. %218040 COSTELLO SYNDROME Later these cases were diagnosed as costello syndrome (Der Kaloustian, 1993; The hypothesis of autosomal recessive inheritance of costello syndrome was http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:218040] -e

66. PHP : Resource Details , costello syndrome is a very rare genetic disorder with approximately 150 reported cases......International costello syndrome Support Group (UK) http://www.php.com/include/agency/agency_item.php?AgencyID=2134&where_keywords=

67. Support Group Resources International costello syndrome Support Group costello syndrome is a very rare genetic disorder with approximately 150 reported cases world wide. http://disability-resource.com/osupp.html

Support Group Resources Local Support Groups National and International Support Groups Translate this page into French German Italian Norwegian ... The Doctor Directory - Find a physician anywhere in the U.S. Lists practice information for 500,000 physicians, 6,500 hospitals, 1,500 health plans and news and information for 30 top level health topics National and International Support Groups ALS (Lou Gehrig's Disease) Support Groups from The ALS Association. Woodland Hills, California 91364 U.S.A. American Self-Help Clearinghouse Database and hotlinks to over 800 national/int'l/model member-run support groups; registry for parents interested in starting a needed new national/int'l support network that doesn't presently exist; and local self-help group clearinghouses worldwide. Australian Reflex Sympathetic Dystrophy Support Group (RSD)(CRPS) Breast Cancer Support How to Find a Breast Cancer Support Group. CFIDS CFS FMS M.E. GWS Directory A Directory of Support Groups and Information pertaining to these medical conditions. Info for patients, physicians, friends, family, employers, insurers, and advocates. CFIDS/FMS/M.E. Directory

68. KMOV.com | St. Louis, MO | Health A New Zealand doctor identified costello syndrome in 1987. costello syndrome alters physical features but can also affect the heart, a child s ability http://www.kmov.com/health/health_stories/stories/kmov_health_050622_costellosyn

Health St. Louis, Missouri Customize Make this your home page E-mail newsletters MySpecialsDirect ... E-mail it to a friend News 4 Health Team: Costello Syndrome 05:40 PM CDT on Wednesday, June 22, 2005 KMOV (KMOV) From the day she was born Ray Gardiner and his wife wondered and worried about what was making their daughter, Claire. Costello Syndrome alters physical features but can also affect the heart, a child's ability to eat and cause mental retardation. This text is invisible on the page, but this text is affected by the invisible item's flow. This text is invisible on the page, but this text is affected by the invisible item's flow. This text is invisible on the page, but this text is affected by the invisible item's flow. More headlines... Illinois expands stem cell research invitation St. Louis medical community to help hurricane victims Missouri can stop paying for certain medical equipment ... More... ARTICLE TOOLS: Print it Discuss it E-mail it to a friend Advertising Find a car Find a dealer Sell Your Car Half Price Menu Deals!

69. Current Opinion In Cardiology - UserLogin Exclusion of PTPN11 mutations in costello syndrome further evidence for distinct etiologies of Noonan, cardiofacio-cutaneous, and costello syndromes. http://www.co-cardiology.com/pt/re/cocardio/fulltext.00001573-200403000-00007.ht

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70. Congenital, Hereditary, And Neonatal Diseases And Abnormalities Hereditary, and Neonatal Diseases and Abnormalities costello syndrome (not on MeSH) - Cri-du-Chat Syndrome - Cri-du-Chat Syndrome - Cri-du-Chat http://www.mic.ki.se/Diseases/c16.html

search search staff sitemap ABOUT KAROLINSKA INSTITUTET ... print this page Diseases and Disorders Links pertaining to Congenital, Hereditary, and Neonatal Diseases and Abnormalities Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Abnormalities Aicardi Syndrome (not on MeSH) Amniotic Band Syndrome Anencephaly ... Wolf-Hirschhorn Syndrome (not on MeSH) Congenital, Hereditary, and Neonatal Diseases and Abnormalities The US National Organization for Rare Disorders , including a Rare Disease Database , and a List of Disease-specific Organizations Search Jablonski's MCA/MR Syndromes Database -NOTE: info may be outdated!! [Congenital Abnormalities associated with Mental Retardation] - NLM (US) Indice delle malattie [in Italian] - InformaGene (IT) A Short History of Mapping [B Mertz] - Access Excellence GENATLAS: Pathology Search [J Frezal] - Univ Rene Descartes, Paris (FR) OrphaNet [rare diseases] - (FR) A Birth Disorder Information Directory - Spamgid.com

71. Tumor Predisposition Syndromes costello syndrome diaphyseal medullary stenosis with malignant fibrous histiocytoma Cockayne syndrome. congenital neutropenia. costello syndrome http://www.humpath.com/article.php3?id_article=360

72. Canadian Directory Of Genetic Support Groups International costello syndrome Support Group (costello syndrome) International Dyslexia Association (Dyslexia) International Fibrodysplasia Ossificans http://www.lhsc.on.ca/programs/medgenet/i_sup.htm

Index by support group Canadian Directory of Genetic Support Groups Immune Deficiency Foundation (Immune Deficiency Disorders, Severe Combined Immunodeficiency Syndrome) Incontinentia Pigmenti International Foundation (Incontinentia Pigmenti) International Children's Anophthalamia Network (Anophthamia, Microphthalmia) International Costello Syndrome Support Group (Costello Syndrome) International Dyslexia Association (Dyslexia) International Fibrodysplasia Ossificans Progressiva (FOP) Association (Fibrodysplasis Ossificans Progressiva) International Joseph Diseases Foundation Inc. (Joseph's Disease) International Lesch-Nyhan Disease Association (Lesch-Nyhan Disease) International Organization for Glutaric Aciduria (Glutaric Aciduria, Type I) International Progeria Registry (Progeria) (Alpha Mannosidosis, Aspartylglucosaminuria, Beta Mannosidosis, Fucosidosis, Galactosialidosis, Sialidosis, Schindler Disease)

73. The Advertiser - Award For Child Who Beat The Odds But Cath says the need to raise awareness of costello syndrome is still vitally And the very first costello syndrome Clinic has just been opened in http://www.nemadvertiser.co.uk/news/w/124/124973_award_for_child_who_beat_the_od

Contact Us Site Map Contents News News Archive Home Features ... - Public Transport News 09 September 2005 email to a friend Published: 14th January 2005 Award for child who beat the odds HELAINA Stone with mum Cath and dad Colin. A LOCAL youngster who beat the odds of surviving life threatening health problems has been honoured by a national charity. Courageous ten-year-old, Helaina Stone, from New Moston has been officially named a Little Star by Cancer Research UK after surviving stomach cancer, brain surgery and coping with Costello Syndrome, a rare genetic condition. The poorly youngster was diagnosed with the condition at three months old, and two years later developed her first bout of cancer, during which doctors said she only had a ten per cent chance of survival. But despite fighting back against the odds, Helaina faced treatment for a second tumour in exactly the same place, just 14 months after her recovery. In addition to these setbacks, the Camberwell Special School Pupil underwent a hysterectomy at the age of five, brain surgery and metal rods being placed in her spine, which had become twisted after she developed scoliosis. But little Helaina's will to survive overpowered the problems she has encountered, and she has developed passions for dancing, horse riding, Rainbows and drama classes which led to a part as an extra in teen soap Hollyoaks.

74. Health Library - 12.31.13.113/library/healthguide/enus/SelfHelp/to Pediatrics THE FUNCTIONAL HEALTH STATUS AND ORTHOPAEDIC MD, Michael J. Goldberg, MD, FAAP, with the costello syndrome Study Group. Department of Orthopaedic Surgery, Tufts-New England Medical Center Hospital, http://12.31.13.113/library/healthguide/en-us/illnessconditions/topic.asp?hwid=n

75. Resources For Genetic Counselors - Beckwith-Wiedemann Syndrome costello syndrome this syndrome resembles BWS only in the neonatal period, Children with costello syndrome have very coarse facial features and failure http://www.genesoc.com/counseling2/article22.html

Modules Home FAQ Feedback Forums ... Your Account Who's Online There are currently, 6 guest(s) and 2 member(s) that are online. You are Anonymous user. You can register for free by clicking here Languages Select Interface Language: Albanian Arabic Brazilian Catala Chinese Czech Danish Dutch English Euskara Finnish French Galego German Greek Hungarian Icelandic Indonesian Italian Macedonian Norwegian Polish Portuguese Romanian Russian Slovak Slovenian Spanish Swedish Thai Turkish Ukrainian Vietnamese Login Nickname Password Security Code: Type Security Code Don't have an account yet? You can create one . As a registered user you have some advantages like theme manager, comments configuration and post comments with your name. Old Articles Thursday, February 10 VATER Association Turner Syndrome Tuberous Sclerosis Trisomy 18 ... Older Articles Beckwith-Wiedemann syndrome Posted on Monday, February 07 @ 21:40:42 CST by debi Beckwith-Wiedemann Syndrome (Jan 2003) Overview: Disorder of growth characterized by macrosomia (large body size), macroglossia (large tongue), visceromegaly(large organs), omphalocele, neonatal hypoglycemia, ear creases/pits embryonal tumors (i.e., Wilms tumor (kidney tumor), hepatoblastoma (liver tumor), and less commonly neuroblastoma, rhabdomyosarcoma). Genetic Etiology Mode of inheritance o Usually sporadic o ~85% have negative family history 15% have history consistent with AD inheritance with incomplete penetrance and preferential maternal transmission o Believed to be a multigenic disorder caused by alterations in growth regulatory genes on chromosome 11p15

76. The Turkish Journal Of Pediatrics 15) Platton MA, Baraitser M. Cutis laxa and the costello syndrome (Letter). costello syndrome natural history and differential diagnosis of cutis laxa. http://tjp.dergisi.org/text.php3?id=86

77. Health Library - 12.42.224.150/library/healthguide/enus/illnesscon www.rarediseases.org/search/rdbdetail_abstract.htm Nemours.org - Application process - Alfred I. duPont Hospital for Adaptive skills, cognitive and behavioral characteristics of costello syndrome. and Behavioral Functioning in Patients with costello syndrome. http://12.42.224.150/library/healthguide/en-us/SelfHelp/topic.asp?hwid=shc29cos

78. Title Adaptive Functioning Competence/ Cognitive Ability/ costello syndrome. 5036. Clark, R., Dogan, RR, Akbar, NJ Youth and parental correlates of http://www.aseba.org/products/adaptive_functioning_&_competence.htm

Bibliography of Published Studies Using ASEBA Materials 4001. Achenbach, T.M., Rescorla, L.A. 4002. Achenbach, T.M., Rescorla, L.A. 4053. Booth, C.L., Kelly, J.F. Child care effects on the development of toddlers with special needs. Early Childhood Res Q, 4232. Karver, M., Bickman, L. Positive functioning: Does it add validity to maladaptive functioning items? Evaluation and Program Planning, 4377. Price, C.S., Spence, S.H., Sheffield, J., Donovan, C. The development and psychometric properties of a measure of social and adaptive functioning for children and adolescents. J Clin Child Adolesc Psychol, 4478. Torquati, J.C., Gamble, W.C. Social resources and psychosocial adaptation of homeless school aged children. J Soc Distress Homeless, 4689. Jeong, S.W. The influence of original family relationship on psychosocial adaptation of adolescents in institutional care. J Korean Society Child Welfare, 4718. Kolaitis, G., Tsiantis, J., Madianos, M., Kotsopoulos, S. Psychosocial adaptation of immigrant Greek children from the former Soviet Union. European Child and Adolescent Psychiatry

79. Link Directory - Finnish Information Center On Mental Retardation costello syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes Costello Kids, International costello syndrome Support Group http://www.saunalahti.fi/kup/engl/webs_c.html

Finnish Information Center on Mental Retardation English links A B C D ... Z CAHMR Syndrome cataract-hypertrichosis-mental retardation (CAHMR) syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes, Stanley Jablonski 1999 CAHMR SYNDROME, OMIM, Victor A. McKusick Cataract hypertrichosis mental retardation, Orphanet Cataract, hypertrichosis, and mental retardation (CAHMR): a new autosomal recessive syndrome, Temtamy SA, Sinbawy AH, Am J Med Genet. 1991 Dec 15;41(4):432-3 - PubMed CAMFAK Syndrome CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME, OMIM, Victor A. McKusick CAMFAK (cataract-microcephaly-failure to thrive-kyphoscoliosis) syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes, Stanley Jablonski 1999 Camfak syndrome, Orphanet, E. Robert-Gnansia A syndrome of microcephaly and cataracts in four siblings. A new genetic syndrome? Scott-Emuakpor AB, Heffelfinger J, Higgins JV, ... 1989 Oct;34(2):194-8 - PubMed Cantú Syndrome Cantú syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY, OMIM, Victor A. McKusick Keratosis follicularis dwarfism cerebral atrophy, Orphanet Cardiofaciocutaneous Syndrome Cardiofaciocutaneous Syndrome, NORD

80. 04.26.2004 costello syndrome. costello syndrome Support Group (UK) costello syndrome NORD costello syndrome-case report. CREST Syndrome http://genetics.rusmedserv.com/catalog/syndlist/

Genetic Catalog SYNDROMES (alfabetical list) Genetic Catalog GENERAL ASPECTS HISTORY EUGENICS ... PRIVATE SYNDROMOLOGY SYNDROMES (alfabetical list) SCREENING OF THE INHERITED METABOLIC DISEASES GENETIC COUNSELLING PRENATAL DIAGNOSIS PREIMPLANTATION DIAGNOSIS ... Case Genetic Reports Search Genetics: åíåòèêà ÷åëîâåêà online Genetic Center E-mail: SYNDROMES (alfabetical list) A B C D ... Z A Aarskog syndrome Aarskog-Scott syndrome-OMIM 305400 Aarskog syndrome-Online and Offline Support A Aarskog syndrome-support groups-Kansas Univ. AARSKOGS syndrome-PedBase ... Aarskog syndrome-Support Groups Aase syndrome Aase syndrome - Pediatric Encyclopedia Acanthosis Nigricans Acanthosis Nigricans Maligna-DermIS Online Atlas Acanthosis Nigricans Benigna-DermIS Online Atlas Achondrogenesis Achondrogenesis - NORD Achondroplasia Achondroplasia Achondroplasia-Baby Net Achondroplasia (rev1998) Achondroplasia-Photo-Medical Genetics ... Health Supervision for Children With Achondroplasia (RE9514) Acrodermatitis Enteropathica Acrodermatitis enteropathica-DermIS Online Atlas Acrodysostosis Acrodysostosis - Pediatric Encyclopedia Acrodysostosis - NORD Acromegaly Acromegaly-DermIS Online Atlas Acromesomelic Dysplasia Acromesomelic Dysplasia - NORD (abstract) Acromicric Dysplasia Acromicric Dysplasia - NORD ADAM COMPLEX

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