21. Noonan Syndrome noonan syndrome Fact Sheet by IBIS. The disorder now known as noonan syndrome bears similarities to the disorder described by Turner (1938) and shown by http://ibis-birthdefects.org/start/noonan.htm

Tips for printing Noonan Syndrome About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Please Explore: Support Groups Professional Associations Key Information Sources Topics include Title and Male Turner Syndrome Noonan Syndrom Noonan Syndrome Noonanovej Syndròm Pseudo-Turner Syndrome Pterigium Colli Syndrome Sindrome di Noonan Turner-Like Syndrome Turner Phenotype with Normal Karyotype Watson Syndrome (Neurofibromatosis) Special Resources Noonan Syndrome A Selection of Internet Sites [*] Outstanding [P] Professionals [S] Support Groups [Italian] [Slovakian] [Danish] [German] [Norwegian] [*][P] Noonan syndrome 1; NS1 OMIM. The disorder now known as Noonan syndrome bears similarities to the disorder described by Turner (1938) and shown by Ford et al. (1959) to have its basis in a 45,X chromosomal aberration ... Noonan (1968) reported 19 cases of whom 17 had pulmonary stenosis and 2 had patent ductus arteriosus. Twelve were males and 7 were females. Deformity of the sternum with precocious closure of sutures was a frequent feature .. [*][P] Noonan Syndrome Birth Defects Foundation. Noonan Syndrome Booklet. This booklet, is intended for individuals with Noonan Syndrome, parents, professionals and friends. It has been produced to encourage greater awareness, and provide a brief overview of current available information ...

22. Glossary GLOSSARY OF MEDICAL TERMS PHRASES RELATING TO noonan syndrome http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

23. Noonan Syndrome noonan syndrome affected children may show no obvious signs to the onlooker, but the problems may be many and complex with no clinical test http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

24. Noonan Syndrome / Family Village Library Learn More About It * Web Sites * Search Google for noonan syndrome The noonan syndrome Support Group, Inc. is committed to providing support, http://www.familyvillage.wisc.edu/lib_noon.htm

Noonan Syndrome Who to Contact Where to Go to Chat with Others Learn More About It Web Sites ... Search Google for "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: info@noonansyndrome.org Web: http://www.noonansyndrome.org/ The Noonan Syndrome Support Group, Inc. is committed to providing support, current information, and understanding to those affected by Noonan syndrome and its associated anomalies. It is also our goal to raise the awareness of, and educate the medical community as to the complex nature of this syndrome and how it affects the lives of those who have it. With the help of our members from around the world we hope to be able to provide further research into the areas of symptoms, diagnosis, treatment and outcomes related to Noonan syndrome. We recognize the importance of linking patients, specialists, and researchers from around the world to improve our understanding of this disease and are committed to helping establish connection across the globe. The Group is intended for people whose lives are touched by Noonan Syndrome, and want to exchange experiences and hopes regarding our children (or us). Associated professionals are also welcome. We offer support, networking and information. We aim to create greater awareness amongst professionals and the public at large. We support research into the many aspects of this complex condition.

25. BBC - Health - Ask The Doctor - Noonan's Syndrome A look at the different ways Noonan's syndrome affects people. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

26. Noonan Syndrome noonan syndrome is inherited as an autosomal dominant condition. A gene for noonan syndrome (NS1) has been mapped to chromosome number 12. http://www.manbir-online.com/diseases/noonan.htm

Sorry, your browser doesn't suppor Java. Noonan Syndrome Synonynms webbed neck syndrome male Turner syndrome female pseudo-Turner syndrome Jacqueline Noonan, paediatrician and heart specialist in 1963, published a report on a small group of patients with typical facies, congenital heart defect, and some clinical features similar to Turner syndrome, but with normal chromosomes. Its after her that this syndrome has been named. Noonan syndrome is inherited as an autosomal dominant condition. This means that the Noonan gene is on a non-sex (autosomal) chromosome and is transmitted from parent with a 50% probability to child. Although one dose of the Noonan gene is enough to cause the syndrome. A gene for Noonan syndrome (NS1) has been mapped to chromosome number 12. There are several different Noonan genes. The frequency of the Noonan syndrome is estimated to be between 1:1,000 and 1:2,500 in the general population Main features of this syndrome are: Pulmonary Stenosis Short stature after birth Webbing of Neck Caved in Chest Bones In boys, Testes that do not descend into the scrotum

27. National Library Of Medicine Includes the alternate names, a summary and a list of major features for noonan syndrome. http://www.nlm.nih.gov/cgi/jablonski/syndrome_cgi?term=Noonan syndrome&field

28. Noonan Syndrome - Health And Medical Information Produced By Doctors - MedicineN Doctorproduced health and medical information written for you to make informed decisions about your health concerns. http://www.medicinenet.com/noonan_syndrome/article.htm

document.writeln(''); MedicineNet Home > Noonan Syndrome search help Printer-Friendly Format FREE Newsletters Email to a Friend ... Next Noonan Syndrome What is Noonan syndrome? Why is it named Noonan syndrome? What did Noonan syndrome used to be called? (obsolete terms) What are the body features of Noonan syndrome? ... Noonan Syndrome At A Glance What is Noonan syndrome? Noonan syndrome is a multifaceted condition characterized by a series of birth defects (congenital malformations) including short stature after birth (postnatal growth retardation ), webbing of the neck (pterygium colli), caved-in chestbone (pectus excavatum), narrowing of the artery from the heart to the lungs (pulmonic stenosis) and, in boys, testes that do not descend normally into the scrotum (cryptorchidism). Why is it named Noonan syndrome? The accepted name of this disorder is Noonan syndrome. It is named after Dr. Jacqueline A. Noonan who in 1968 reported 19 cases with the condition including 17 with narrowing of the artery to the lungs (pulmonary stenosis). Twelve of Dr. Noonan's patients were male and 7 were female. Noonan was clearly not the first person to discover the condition that bears her name today. In 1883 Kobilinsky reported a young man with webbing of the neck and several other features suggestive of Noonan syndrome and in 1928 Weissenberg provided a full and unmistakable description of the disease. Noonan, in collaboration with D. A. Ehmke, rediscovered the condition and noted the association with pulmonic stenosis.

29. Health And Medical Information Produced By Doctors - MedicineNet.com noonan syndrome Related Diseases Conditions noonan syndrome Related Doctor s Views Updates Doctor s Responses about noonan syndrome http://www.medicinenet.com/noonan_syndrome/

document.writeln(''); MedicineNet Home search help What's Inside the Noonan Syndrome Health Center Noonan Syndrome Main Article 2 Doctor's Views related to Noonan Syndrome 1 Health Features related to Noonan Syndrome Noonan Syndrome RSS feed Our Noonan Syndrome Main Article provides a comprehensive look at the who, what, when and how of Noonan Syndrome Digestion Newsletter How to Choose a Doctor Join the discussion on the Digestion Message Boards Noonan Syndrome related Doctor's Views Doctor: Getting the Most from Your Doctor’s Appointment How to Choose a Doctor Noonan Syndrome related Health Features Doctor: Checklist to Take To Your Doctor's Appointment Terms related to Noonan Syndrome: Medications MedTerms Medical Dictionary Home Help ... Content Solutions Allergies Alzheimer's Arthritis Asthma Blood Pressure Cancer Cholesterol Chronic Pain Crohn's Disease Depression Diabetes Dictionary Digestion Eyesight First Aid Healthy Kids Healthy Living Heart Hepatitis C HIV/AIDS Liver Lung Cond. Medications Menopause Men's Health Mental Health Migraine Osteoporosis Rheum. Arthritis

30. Noonan Syndrome noonan syndrome is a genetic disorder that causes abnormal development of multiple parts of the body. In particular there is webbing of the neck and http://www.healthcentral.com/ency/408/001656.html

Dr. Dean TV Specials Newsletters Home ... Health Tools Search Choose a Health Topic * All Health Topics * Acne Addictions AIDS/HIV Alcohol Abuse Allergies Alternative Medicine Alzheimer's Arthritis Asthma Attention Deficit Disorder (ADHD) Backache Bipolar Affective Disorder Birth Control Blood Blood Pressure Bone/Joint/Tendon Bowel Brain Breast cancer Cancer Cerebral Palsy Cholesterol Cramps Crohn's Disease Cysts Dental/Oral Depression Diabetes Diet, Fitness, Looks Disabled/Special Needs Drug Abuse Ear/Nose/Throat Eating/Appetite Eczema Encephalitis Eye/Vision Fatigue Fever Flu Food Poisoning Foot Gallbladder Gastrointestinal Genetic/Congenital GERD/Heartburn Hair Loss Hair/Scalp Headache Hearing Heart Disease, Stroke Heat/Sunstroke Hepatitis Hernia Herpes High Blood Pressure Hormonal Immune Disorders Immunizations/Vaccines Impotence Incontinence/Bladder Infections Injuries Kidney/Urinary Kids Learning Disabilities Liver Lung Cancer Men Menopause, Postmenopause Migraine Mobility/Balance Multiple Sclerosis Muscle Neural Nosebleeds Pain Parasites Pituitary PMS Pregnancy Prostate Cancer Prostate Disorders Psoriasis Psychological Raynaud's Disease Respiratory Reye Syndrome Rheumatoid Arthritis Schizophrenia Seniors Sensory Sexually Transmitted Disease Skin Sleep Speech Disorders Spinal Thyroid Trauma Weight Loss Women Yeast Infections Home Health Encyclopedia Noonan syndrome Noonan syndrome Injury Disease Nutrition Poison ... Prevention Noonan syndrome Definition: Noonan syndrome is a genetic disorder 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.

31. GeneReviews: Noonan Syndrome Your browser does not support HTML frames so you must view noonan syndrome in a slightly less readable form. Please follow this link to do so. http://www.genetests.org/query?dz=noonan

32. Noonan Syndrome - Genetics Home Reference Where can I find additional information about noonan syndrome? What if I still have specific questions about noonan syndrome? http://ghr.nlm.nih.gov/condition=noonansyndrome

Home What's New Browse Handbook ... Search Noonan syndrome Related Gene(s) Quick links to this topic MedlinePlus Health Information Educational resources Information pages Patient support For patients and families Gene Reviews Clinical summary Gene Tests DNA test labs PubMed Recent literature OMIM Genetic disorder catalog References Noonan syndrome On this page: What is Noonan syndrome? How common is Noonan syndrome? ... help with understanding Noonan syndrome? What is Noonan syndrome? Noonan syndrome is a developmental disorder characterized by unusual facial characteristics, short stature, heart defects, bleeding problems, and skeletal malformations. Eye abnormalities can occur in up to 95 percent of patients. Problems with language and speech are common. Most males with this disorder have undescended testicles (cryptorchidism). The majority of children diagnosed with Noonan syndrome have normal intelligence, but a small percentage have special educational needs, and some affected individuals are mildly mentally retarded. How common is Noonan syndrome?

33. Noonan Syndrome Support Group, Inc. The noonan syndrome Support Group has moved to http//noonansyndrome.org. http://www.geocities.com/~noonansyndrome/

The Noonan Syndrome Support Group has moved to http://noonansyndrome.org

34. BDF Newlife - Birth Defects Children's Charity - What Is Noonan Syndrome noonan syndrome is known as “the most complex genetic disorder”. noonan syndrome was first named in 1963 by Dr Jacqueline Noonan, a Paediatric http://www.bdfcharity.co.uk/docs/family_patients_area/noonan_1.htm

What is Noonan Syndrome? Noonan Syndrome was first named in 1963 by Dr Jacqueline Noonan, a Paediatric Cardiologist in the United States. It is a genetic condition, affecting males and females equally. Although it is primarily an inherited condition, in about 50% of cases it can occur in a family from a genetic mutation. Noonan Syndrome and BDF Newlife The Unit was established in 1987 and is recognised as the leading international centre for NS research. Results of its research have been published and presented internationally and have contributed significantly to the basis of contemporary understanding and treatment. Indeed, the Unit, in collaboration with teams in Holland and the USA, has identified the gene responsible for the condition, which means that a diagnostic test can now be developed. What are the features of Noonan Syndrome Features vary in the degree of severity between individuals and families. Not everyone with Noonan Syndrome will exhibit all features. Indeed, often once a child is diagnosed, a parent or even a grandparent is then diagnosed. Noonan Syndrome can cause congenital heart disease, short stature, genital abnormalities and in some cases, learning difficulties.

35. Cleft And Craniofacial Anomalies: Noonan Syndrome The noonan syndrome features are easier to see at birth and by adulthood they are Children with noonan syndrome may have a coagulation abnormality. http://www.ucdmc.ucdavis.edu/children/services/cleft/health/anomalies/noonan.htm

For Health Consumers For Health Professionals Find a Clinic Find a Doctor ... Employment Noonan Syndrome It is thought that this Syndrome occurs in somewhere between 1/1,000 and 1/ 2,500 newborn babies. The Noonan Syndrome features are easier to see at birth and by adulthood they are often very subtle and can easily be missed. What are the features of Noonan Syndrome? More serious problems include a smaller than normal jaw. This can create some feeding problems, and even in some cases lead to failure to thrive. Babies with this syndrome are also at an increased risk of cardiac defects. It is important to have a cardiac evaluation if Noonan Syndrome is diagnosed. Children with Noonan Syndrome may have a coagulation abnormality. This means that the blood may not clot as quickly as it should. There is a wide range in coagulation differences, ranging from more serious problems of clotting after surgery, to easy bruising, and even to an abnormality seen in the laboratory with no known clinical consequences. Can surgery help?

36. Noonan's Syndrome (www.whonamedit.com) Noonan s syndrome A complex familial syndrome similar to Turner’s, with the Turner phenotype, but there is no chromosomal defect and noonan syndrome occurs http://www.whonamedit.com/synd.cfm/1920.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Noonan's syndrome Also known as: Familial Turner syndrome Female pseudo Turner syndrome Pseudo Turner syndrome Male Turner syndrome Pseudo Ullrich-Turner syndrome Turner-like syndrome Turner's phenotype with normal karotype Turner's syndrome in female with X-chromosome Ullrich-Noonan syndrome XX Turner phenotype syndrome Turner phenotype syndrome Associated persons: Jacqueline Anne Noonan Otto Ullrich Description: Jacquline A. Noonan and Dorothy Ehmke [American cardiologist/paediatrician] in 1963 defined the syndrome on the basis of clinical and cytogenetic findings in six boys and three girls with valvular pulmonary stenosis, short stature, hypertelorism and skeletal anomalies, and, in boys, retentio testis. In a later publication (1968) Noonan described a total of 19 patients of both sexes with unusual facies, congenital heart defect and other symptoms resembling those of Turner’s syndrome. However, the patients had normal chromosomes.

37. Noonan Syndrome noonan syndrome is a genetic condition which has an incidence rate of Jan and Tom Irvine are forming a noonan syndrome Support Group for Arizona. http://www.vibrationdata.com/noonan.htm

Noonan Syndrome Support Group of Arizona Daniel at 5 years old FACTS Noonan syndrome is a genetic condition which has an incidence rate of: 1/1,000-1/2,500 live births. It can occur in both males and females. Noonan syndrome is similar to Turner syndrome. Characteristics may include: congenital heart disease, short stature, distinctive facial features, dental problems, bruising, bleeding, and learning difficulties. The facial features may include: low-set or rotated ears, and Hypertelorism (widely spaced eyes). Another characteristic is "Pectus excavatum," which is a concave shape in the chest. Children with Noonan syndrome may have some, or all, of the characteristics. All children with Noonan syndrome should see a cardiologist and have an ultrasound examination of the heart chambers and valves. CONTACT Jan and Tom Irvine are forming a Noonan Syndrome Support Group for Arizona. Your participation is welcome. Please call Jan Irvine at 480-752-9975. Or please send an Email via: tomirvine@aol.com

38. Noonan Syndrome noonan syndrome is a rare genetic disorder that is typically evident at birth (congenital). The disorder http://my.webmd.com/hw/raising_a_family/nord412.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Noonan Syndrome Important It is possible that the main title of the report Noonan Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Female Pseudo-Turner Syndrome Male Turner Syndrome Turner Phenotype with Normal Chromosomes (Karyotype) NS Disorder Subdivisions None General Discussion In some affected individuals, Noonan syndrome appears to result from spontaneous (sporadic) genetic changes (mutations). In others, the disorder may be transmitted as an autosomal dominant trait. Genetic analysis of one affected multigenerational family (kindred) suggests that the disorder may result from mutations of a gene located on the long arm (q) of chromosome 12 (12q24). However, many investigators indicate that Noonan syndrome may be caused by mutations of different genes (genetic heterogeneity). Resources Human Growth Foundation 997 Glen Cove Avenue Glen Head, NY 11545

39. Noonan Syndrome International network. Founded 1996. Provides information for persons with noonan syndrome, their families, http://my.webmd.com/hw/raising_a_family/shc29noo.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... Noonan Syndrome Support Group Noonan Syndrome Noonan Syndrome Support Group International network. Founded 1996. Provides information for persons with Noonan syndrome, their families, and interested others. Networks individuals together for peer support. Information and referrals, speakers bureau, phone help. WRITE: Noonan Synd. Support Group P.O. Box 145 Upperco, MD 21155 CALL: 1-888-686-2224 E-MAIL: Wander@bellatlantic.net WEBSITE: http://www.noonansyndrome.org VERIFIED: 5/6/2005 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

40. ► Noonan Syndrome A medical encycopedia article on the topic noonan syndrome. http://www.umm.edu/ency/article/001656.htm

var MenuLinkedBy='AllWebMenus [2]', awmBN='530'; awmAltUrl=''; Disease Nutrition Surgery Symptoms Injury ... Z Maryland Medical Center Programs Maryland Heart Center Home Medical Reference Encyclopedia (English) Toggle English Spanish Noonan syndrome Overview Symptoms Treatment Prevention 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

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