41. 1Up Health > Noonan Syndrome > Causes, Incidence, And Risk Factors Of Noonan Syn Comprehesive information on noonan syndrome (Turnerlike syndrome of males). Noonansyndrome Causes, Incidence, and Risk Factors. Alternative names http://www.1uphealth.com/health/noonan_syndrome_info.html

1Up Health Noonan syndrome Alternative Medicine Clinical Trials ... Health Topics A-Z Search 1Up Health Noonan syndrome Information Noonan syndrome Causes, Incidence, and Risk Factors Alternative names : Turner-like syndrome of males Definition : A genetic syndrome that causes abnormal development of multiple parts of the body. In particular there is webbing of the neck and different shapes to the chest that are reminiscent of Turner syndrome, hence the former name Turner-like syndrome. Causes, Incidence, and Risk Factors Noonan syndrome can be inherited in an autosomal dominant manner. It affects at least 1 in 2,500 children. The fact that some children do not have a parent with Noonan syndrome likely reflects sporadic inheritance, i.e., presumably the occurrence of a new mutation. The first specific gene that causes Noonan syndrome, called PTPN11, was discovered in 2001. It is expected that other genes will be discovered that cause Noonan syndrome. Frequently seen abnormalities include webbing of the neck, changes in the sternum (usually a sunken chest called pectus excavatum), facial abnormalities, and congenital heart disease (especially pulmonic stenosis ). Because these abnormalities resemble those of Turner syndrome (which only affects females), Noonan syndrome used to be called "male Turner syndrome", this term is not used because Noonan syndrome can affect females also.

42. 1Up Health > Noonan Syndrome (Turner-like Syndrome Of Males) Information Comprehesive information on noonan syndrome (Turnerlike syndromeof males). 1Up Health Diseases Conditions noonan syndrome. http://www.1uphealth.com/health/noonan_syndrome.html

1Up Health Alternative Medicine Clinical Trials Health News ... Health Topics A-Z Search 1Up Health Noonan syndrome Information Guide Alternative names : Turner-like syndrome of males Definition : A genetic syndrome that causes abnormal development of multiple parts of the body. In particular there is webbing of the neck and different shapes to the chest that are reminiscent of Turner syndrome, hence the former name Turner-like syndrome. Jump to a Section of this Guide Definition Causes, Incidence, and Risk Factors Symptoms Prevention ... Calling your Health Care Provider Related Tools and Utilities Search Books on Amazon: Read Articles on eLibrary: Health Products on drugstore.com: Atrial septal defect Heart disease Mental retardation Ptosis ... More More Topics Hearing loss Penis Short stature Testes ... More Search 1Up Health A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's accreditation program is the first of its kind, requiring compliance with 53 standards of quality and accountability, verified by independent audit. A.D.A.M. is among the first to achieve this important distinction for online health information and services. Learn more about A.D.A.M.'s editorial reviewers . A.D.A.M. is also a founding member of Hi-Ethics (www.hiethics.com) and subscribes to the principles of the Health on the Net Foundation (www.hon.ch). Home Contact Us Privacy Links Directory

43. GGRC - Medical Care Information and Causes. noonan syndrome (NS) is a multiplecongenital anomaly syndrome inherited in an autosomal dominant pattern....... noonan syndrome Background. http://www.ddhealthinfo.org/ggrc/doc2.asp?ParentID=5195

44. PTPN11 Mutation In A Large Family With Noonan Syndrome And Dizygous Twinning Short Report. PTPN11 mutation in a large family with noonan syndrome and dizygoustwinning. noonan syndrome; cardiofacio-cutaneous syndrome; PTPN11; DHPLC. http://www.nature.com/cgi-taf/DynaPage.taf?file=/ejhg/journal/v11/n1/full/520091

45. Noonan Syndrome noonan syndrome. Who to Contact The noonan syndrome Support Group, Inc. Where to Goto Chat with Others NOONANSYNDROME noonan syndrome e-mail disscussion list. http://www.communicationdisorders.net/Noonansyndrome.html

Noonan Syndrome Who to Contact The Noonan Syndrome Support Group, Inc. P.O. Box 145 Upperco, MD. 21155 USA 888-686-2224 (U.S.) 410-374-5245 (all others) E-mail: wandar@bellatlantic.net Where to Go to Chat with Others NOONAN-SYNDROME Noonan Syndrome e-mail disscussion list. To subscribe, send a message to: listserv@home.ease.lsoft.com In the body of the message type: SUBSCRIBE NOONAN-SYNDROME Learn More About It Noonan Syndrome Information from Ped Base Noonan Syndrome Information from OMIM Web Sites Noonan Syndrome Support Groups Web Page HOME

46. Noonan Syndrome Articles, Support Groups, And Resources noonan syndrome articles, support groups, and resources for patientsfrom Med Help International (www.medhelp.org). noonan syndrome. http://www.medhelp.org/HealthTopics/Noonan_Syndrome.html

[Health Topics A-Z] A B C D ... Z Noonan Syndrome Support Groups: Noonan Syndrome Support Group [Med Help Home] [Library Search] [Medical Forums] ... [Patient Network] Revised: 3/30/2003

47. Founder Of The Noonan Syndrome Support Group, Inc. Founder of The noonan syndrome Support Group, Inc. Two years ago the Alliance ofGenetic Disorders asked me to become a support group for noonan syndrome. http://www.angelfire.com/md/wandarmd/

Founder of The Noonan Syndrome Support Group, Inc. Hello, My name is Wanda Robinson Visit our web site at: http://www.noonansyndrome.org for more information about Noonan Syndrome. Show your support by ordering the groups pin: http://www.angelfire.com/md/wandarmd/TNSSGPIN.html for more information about the pin. Or call toll free 1-888-686-2224 within the USA or 410-374-5245. Sign My Guestbook View My Guestbook Places to go...... Talking about Wanda TNSSG, Inc. pin picture and information The prayer and wish page The Noonan Syndrome Support Group, Inc. Email: wandar@bellatlantic.net

48. The Noonan Syndrome Prayer And Wish Book The noonan syndrome Prayer and Wish Book. http://www.angelfire.com/md/wandarmd/noonanprayerbook.html

The Noonan Syndrome Prayer and Wish Book Sign The Noonan Syndrome Prayer and Wish book View The Noonan Syndrome Prayer and Wish book Email: wandar@bellatlantic.net

49. Health Library - Noonan Syndrome noonan syndrome. NS. Disorder Subdivisions. None. General Discussion. noonan syndromeis a rare genetic disorder that is typically evident at birth (congenital). http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

50. Noonan Syndrome Homepage Translate this page La sindrome di Noonan è una condizione genetica le cui caratteristiche principalisono costituite da volto peculiare, cardiopatia congenita e bassa statura in http://www.conosciamocimeglio.it/Noonan/index4.htm

HOME AREA NARRATIVA AREA EPIDEMIOLOGICA AREA INFORMATIVA Queste pagine sono rivolte alle persone affette dalla sindrome di Noonan, ai loro familiari, amici e a tutti coloro che si trovano ad operare, in diversi settori, con loro. Il nostro non è un sito puramente informativo ma vuole essere uno strumento di ricerca attraverso l'incontro tra "persone che producono la conoscenza", "ricercatori" e "persone che utilizzano la conoscenza prodotta". legge sulla privacy (art. 10 legge n. 675/96). In un campo in cui ancora le conoscenze sono limitate, riteniamo, che sia fondamentale il contributo di tutti. Se non sei ancora iscritto compila il modulo d'iscrizione Ultimo aggionamento: 12/12/2002 Home Chi siamo Mappa del sito Area narrativa ... FAQ

51. Noonan Syndrome Mappa Translate this page Area informativa Quest'area contiene informazioni generali sulla Sindrome di Noonan,una sezione di aggiornamento della letteratura in cui vengono recensiti e http://www.conosciamocimeglio.it/Noonan/mappa.html

HOME AREA NARRATIVA AREA EPIDEMIOLOGICA AREA INFORMATIVA Mappa del sito Questo sito nasce con un triplice intento: fornire le informazioni attualmente disponibili sulla sindrome e incoraggiare la ricerca clinica per una sempre maggiore conoscenza della condizione ( area informativa area epidemiologica creare una rete di scambio di conoscenze ed esperienze personali tra le famiglie ( area narrativa E' suddiviso in tre aree: Area informativa Area epidemiologica Area narrativa E' il luogo di scambio di esperienze ed emozioni; contiene racconti di vita vissuta scritti da persone con sindrome di Noonan, i loro familiari o altri. ei Difetti timo aggionamento: Home Chi siamo Mappa del sito Area narrativa ... FAQ

52. Health Library - Noonan Syndrome noonan syndrome. NS. Disorder Subdivisions. None. General Discussion. noonan syndromeis a rare genetic disorder that is typically evident at birth (congenital). http://www.laurushealth.com/library/healthguide/illnessconditions/topic.asp?hwid

53. Noonan Syndrome noonan syndrome. Definition noonan syndrome can be inherited in an autosomaldominant manner. It affects at least 1 in 2,500 children. http://www.pennhealth.com/ency/article/001656.htm

Disease Injury Nutrition Poison ... Prevention Noonan syndrome Definition: A genetic syndrome that causes abnormal development of multiple parts of the body. In particular there is webbing of the neck and different shapes to the chest that are reminiscent of Turner syndrome, hence the former name Turner-like syndrome. Alternative Names: Turner-like syndrome of males Causes, incidence, and risk factors: Noonan syndrome can be inherited in an autosomal dominant manner. It affects at least 1 in 2,500 children. The fact that some children do not have a parent with Noonan syndrome likely reflects sporadic inheritance, i.e., presumably the occurrence of a new mutation. The first specific gene that causes Noonan syndrome, called PTPN11, was discovered in 2001. It is expected that other genes will be discovered that cause Noonan syndrome. Frequently seen abnormalities include webbing of the neck, changes in the sternum (usually a sunken chest called pectus excavatum), facial abnormalities, and congenital heart disease (especially pulmonic stenosis ). Because these abnormalities resemble those of Turner syndrome (which only affects females), Noonan syndrome used to be called "male Turner syndrome", this term is not used because Noonan syndrome can affect females also.

54. Short Description Of Cell Lines. Pathology: Turner Syndrome/noonan Syndrome 1 *1 Version 4.200205, Short description of cell lines. Pathology Turnersyndrome/noonan syndrome 1 *163950 OMIM record. By selecting http://www.biotech.ist.unige.it/cldb/pat15.html

Version Short description of cell lines. Pathology: Turner syndrome/noonan syndrome 1 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 Detroit 525 ... By Beatrice...

55. EPEC - Educating Parents Of Extra-special Children - Noonan Syndrome noonan syndrome. noonan syndrome is a rare genetic disorder that is typicallyevident at birth (congenital). The noonan syndrome Support Group, Inc. http://www.epeconline.com/NS.html

Educating Parents of Extra-special Children (EPEC) A resource of information for adults with special needs and parents with special needs children. Noonan Syndrome Noonan syndrome is a rare genetic disorder that is typically evident at birth (congenital). The disorder may be characterized by a wide spectrum of symptoms and physical features that vary greatly in range and severity. In many affected individuals, associated abnormalities include a distinctive facial appearance; a broad or webbed neck; a low hairline in the back of the head; and short stature. Characteristic abnormalities of the head and facial (craniofacial) area may include widely set eyes (ocular hypertelorism); vertical skin folds that may cover the eyes' inner corners (epicanthal folds); drooping of the upper eyelids (ptosis); a small jaw (micrognathia); a low nasal bridge; and low-set, prominent, abnormally rotated ears (pinnae). Distinctive skeletal malformations are also typically present, such as abnormalities of the

56. ORPHANET® : Neurofibromatosis-Noonan Syndrome Translate this page ORPHANET. ORPHANET database access. Neurofibromatosis-Noonansyndrome. Direct access to details Alias Home Page. http://www.orpha.net/static/GB/neurofibromatosis_noonan.html

ORPHANET database access Neurofibromatosis-Noonan syndrome Direct access to details Alias : Home Page

57. ORPHANET® : Noonan Syndrome Translate this page ORPHANET. ORPHANET database access. noonan syndrome. Directaccess to details Alias Pseudo-Turner syndrome. Home Page. http://www.orpha.net/static/GB/noonan.html

ORPHANET database access Noonan syndrome Direct access to details Alias : Home Page

58. NOONAN SYNDROME Features Listed For noonan syndrome. McKusick 163950. Abnormal auditory ossicles;Bleeding diatheses; Cardiomyopathy; Congenital cardiac anomaly, unspecified; http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?1227

59. Midirs Forum - Noonan Syndrome Subject noonan syndrome Created by Vicky Ewins on 23/10/2001 at 085441. ThankyouTopic Responses noonan syndrome (Julie Frohlich 23/10/2001). http://www.midirs.org/midirs/midfourm.nsf/Y12/3152F61A1687263B80256AEE002B75B6

Good Morning and welcome to the MIDIRS Forum. views: Home All Date Category ... Search Subject: Noonan Syndrome Created by Vicky Ewins on 23/10/2001 at 08:54:41. Category: Pregnancy Content: I am a second year midwifery student and am writing an assignment on pre natal screening, focussing on Noonan Syndrome. I would appreciate it if any one could suggest any resources to help me out. Thankyou Topic Responses: Noonan syndrome (Julie Frohlich 23/10/2001) MIDIRS web site is provided for reference information only. MIDIRS is not responsible or liable for any diagnosis made by a user based on the content of the website. Although great care is taken to ensure reference information is both suitable and accurate,MIDIRS is not liable for the contents of any external internet sites referenced, nor does it endorse any commercial product or service mentioned or advised on any of these sites.

60. Midirs Forum Response - Noonan Syndrome Subject noonan syndrome Created by Julie Frohlich on 23/10/2001 at143316. Category Pregnancy Response to noonan syndrome Content http://www.midirs.org/midirs\midfourm.nsf/Y11/533BCCAF5665116580256AEE004A7508?O

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