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Noonan Syndrome: more detail

Noonan Syndrome and Related Disorders - A Matter of Deregulated Ras Signaling (Monographs in Human Genetics)
Noonan Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-04-26
Noonan's Syndrome: A Medical Dictionary, Bibliography, And Annotated Research Guide To Internet References by Icon Health Publications, 2004-12-30
NOONAN-SYNDROME: CHARACTERISTICS, DEVELOPMENT, AND INTERVENTION by STEPHEN VON TETZCHNER, 1998
Noonan-Syndrome:: A New Challenge in Growth Hormone Therapy: Expert Workshop, November 26-28, 2008, Copenhagen, Denmark (Hormone Research from Developmental Endocrinology to Clinical Research)
Noonan syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Deepti, MS, CGC Babu, 2005
Noonan Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
" Another Noonan Connection " by WANDA ROBINSON, 2008

lists with details

Noonan Syndrome (NS) - Medical Dictionary Definitions Of Popular Medical Terms
MedicineNet Home MedTerms medical dictionary AZ List noonan syndrome (NS). Advanced Search. noonan syndrome (NS) Index.
http://www.medterms.com/script/main/art.asp?articlekey=6445
SupportPath.com: Noonan Syndrome
noonan syndrome. noonan syndrome is a rare congenital disorder occuring in males and females. Clinical Trials Research on noonan syndrome None Listed.
http://www.supportpath.com/sl_n/noonan_syndrome.htm

Extractions: Noonan Syndrome is a rare congenital disorder occuring in males and females. It is characterized by short staure, distinctive facial features, and a congenital heart defect (most often Pulmonary Stenosis - narrowing at the pulmonary artery valve). Also called: NS Other topics of interest on SupportPath.com:
Noonan Syndrome - Genetics Home Reference
Genetic disorder catalog. noonan syndrome. What is noonan syndrome? noonan syndrome How common is noonan syndrome? noonan syndrome
http://ghr.nlm.nih.gov/condition=noonansyndrome

Extractions: A service of the U.S. National Library of Medicine Home Search Conditions Genes ... Help Noonan syndrome Noonan syndrome is a developmental disorder characterized by unusual facial characteristics, short stature, heart defects, bleeding problems, and skeletal abnormalities. Most males with this disorder have undescended testicles (cryptorchidism). Noonan syndrome has an incidence of 1 in 1,000 to 2,500 live births. Mutations in the gene cause Noonan syndrome. More than 50 percent of individuals with Noonan syndrome have changes in the PTPN11 gene. Researchers are investigating other genes that might be involved in this syndrome. The PTPN11 gene makes a protein that is important for the proper formation of tissues during development and also plays a role in cell division, cell specialization, and cell movement. Most mutations in the PTPN11 gene cause a change in this protein's sequence of amino acids (the building material of proteins). These changes are believed to cause the protein to be continuously active, rather than switching on and off. The constant activation causes the improper regulation of systems that control cell functions such as growth and division. This misregulation leads to the signs and symptoms of Noonan syndrome.
Www.ddhealthinfo.org - Medical Care Information
and Causes. noonan syndrome (NS) is a multiple congenital anomaly syndrome inherited in an autosomal dominant pattern. noonan syndrome Background.
http://www.ddhealthinfo.org/ggrc/doc2.asp?ParentID=5195
Disease Directory : Genetic Disorders : Noonan Syndrome
Diseases Genetic Disorders noonan syndrome. Birth Defects Foundation noonan syndrome History of the Foundation s involvement with Noonan s.
http://www.diseasedirectory.net/Genetic_Disorders/Noonan_Syndrome/default.aspx

Extractions: Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Noonan Syndrome Archives of NOONAN-SYNDROME@HOME.EASE.LSOFT.COM - Management Help Log off Archive Search. Archives of NOONAN-SYNDROME@HOME.EASE.LSOFT.COM The Noonans Syndrome Support Group, Inc. Birth Defects Foundation: Noonan Syndrome - History of the Foundation's involvement with Noonan's. Printable booklet and newsletter. eMedicine - Noonan Syndrome : Article by Jennifer Ibrahim, MD - Thorough summary of history, diagnosis, and treatment. Founder of The Noonan Syndrome Support Group, Inc. - Founder of The Noonan Syndrome Support Group, Inc. Two years ago the Alliance of Genetic Disorders asked me to become a support group for Noonan Syndrome. Health Information Resource Database: Noonan Syndrome Support ... - Noonan Syndrome Support Group, Inc. Noonan Syndrome News, quarterly newsletter; Members have access to the most recent articles published on Noonan Syndrome. HONselect - Noonan Syndrome - English: Noonan Syndrome, - Turner's Syndrome, Male - Male Turner's Syndrome - Syndrome, Male Turner's - Syndrome, Noonan - Turner Syndrome, Male - Turners National Library of Medicine - Includes the alternate names, a summary and a list of major features for Noonan syndrome.
HONselect - Noonan Syndrome
English noonan syndrome, Turner s Syndrome, Male - Male Turner s Syndrome - Syndrome, Male Turner s - Syndrome, Noonan - Turner Syndrome, Male - Turners
http://www.hon.ch/HONselect/RareDiseases/C05.660.207.690.html
Disease - Noonan Syndrome - Hartford, Connecticut , Saint Francis Care
Disease noonan syndrome - courtesy of Saint Francis Care of Hartford, Connecticut, contemporary medicine with major clinical concentrations in heart disease
http://www.saintfranciscare.com/13069.cfm

Extractions: Back Back to main Health Information page Pectus excavatum 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. Alternative Names: Turner-like syndrome of males Causes And Risk: 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, that is, 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
Health Library -
noonan syndrome. NS. Disorder Subdivisions. None. General Discussion. noonan syndrome is a rare genetic disorder that is typically evident at birth (congenital).
http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=
Noonan Syndrome,Female Pseudo-Turner Syndrome,Male Turner Syndrome,Turner Phenot
noonan syndrome,Female PseudoTurner Syndrome,Male Turner Syndrome,Turner Phenotype with Normal Chromosomes (Karyotype),NS,noonan syndrome,Female Pseudo-Turner
http://www.icomm.ca/geneinfo/noonan.htm

Extractions: National Organization for Rare Disorders 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).
Genetic Disorders, Noonan Syndrome
Submit Your Site to the noonan syndrome category. Sponsored noonan syndrome Sites. Submit Your Site to the noonan syndrome category. Sponsored Results.
http://www.iseekhealth.com/noonan_syndrome-1604.php
University Of Miami School Of Medicine - Glossary - Noonan Syndrome
Diseases and Conditions. noonan syndrome. noonan syndrome. noonan syndrome At A Glance. noonan syndrome is a characteristic constellation of birth defects.
http://www.med.miami.edu/patients/glossary/art.asp?articlekey=6167
Would A 14 1/2year Old, Noonan Syndrome Girl Show A High Reading On Tova Test Fo
Would a 14 1/2year old, noonan syndrome girl show a high reading on tova test for adhd? part of the ADD FAQ. FAQ Farm Health
http://www.faqfarm.com/Health/ADD/24860

Extractions: FAQ Farm Health ADD : Would a 14 1/2year old, noonan syndrome girl show a high reading on tova test for adhd? Would a 14 1/2year old, noonan syndrome girl show a high reading on tova test for adhd? No answer has been contributed to this question yet. Can you help with an answer? Please participate! This ADD question was last updated on May 05, 2004, at 11:14 pm. Popularity in ADD FAQ Question by Barbara P. asked on May 04, 2004, at 10:47 pm. Would a 14 1/2year old, noonan syndrome girl show a high reading on tova test for adhd? : Answers on FAQ Farm are not a substitute for professional advice. For reliable information of any sort you must consult an officially qualified professional in your area. You use this service at your own risk. Please carefully read our Terms of Service If you see inappropriate content please e-mail us at FAQFarm@despammed.com . Include the URL of this page. Thank you! Interaction is what our "question and answer co-op" is all about. Thank you for participating. Recommend 'Would a 14 1/2year old, noonan syndrome girl show a high reading on tova test for adhd? '
Noonan Syndrome
Home Health Conditions and Diseases Genetic Disorders noonan syndrome (9) noonan syndrome Story of 6-year-old Becky, with factsheet and resources.
http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/No

Extractions: See Also: Health: Conditions and Diseases: Rare Disorders The Noonan Syndrome Support Group - Information about this organization as well the disease itself. Offers news, events, a survey, a newsletter and further resources. National Library of Medicine - Includes the alternate names, a summary and a list of major features for Noonan syndrome. Pediatric Database - A definition of Noonam syndrome, the epidemiology, pathogenesis, clinical features, investigations and management. The CaF Directory - A description of Noonan syndrome, its inheritance patterns and pre-natal diagnosing. eMedicine - Noonan Syndrome : Article by Jennifer Ibrahim, MD - Thorough summary of history, diagnosis, and treatment. Birth Defects Foundation: Noonan Syndrome - History of the Foundation's involvement with Noonan's. Printable booklet and newsletter. Noonan Syndrome - Story of 6-year-old Becky, with factsheet and resources. Noonan Syndrome - by Michelle Ellis - Account of her life with the disorder. NORD - Noonan Syndrome - Offers the synonyms, a general discussion and further resources.
Noonan Syndrome Is A Condition, Which Affects Both Children And Adults
noonan syndrome is a condition, which affects both children and adults. We have a daughter, now age 19, with suspected noonan syndrome.
http://www.mkdowney.com/mkd-noonan.htm

Extractions: Noonan Syndrome is a condition, which affects both children and adults. As with other disorders, it affects the person with the disorder and their family as well. We have found valuable resources for support and information as well as learned that "living with" a disability may always be a challenge, but does not have to incapacitate the person or the family. We have a daughter, now age 19, with suspected Noonan Syndrome. Often called a "hidden" condition, the children affected may have no obvious casual signs to the onlooker, but the problems may be many and complex with no clinical test available. Part of our frustration has been the inability to get positive proof of the syndrome, so we, like many others with "suspected NS", learn to manage her health and psychological care by joining groups who have members with similar defined characteristics and behaviors. We take help from as many resources as possible. Noonan Syndrome is a genetic condition that can affect the heart, growth, blood clotting, mental and physical development. Affected individuals may have behavior problems, learning difficulties and many other anomalies. In our daughters case, it was also found in conjunction with Asperger Syndrome. Asperger Syndrome is within the autism spectrum. There are many characteristics within the spectrum and through experience as a mom and educator/speaker I have found many others with Noonan Syndrome who share some of these same autistic/like characteristics as our daughter. For that reason we stay in contact with those having Asperger syndrome as well as those having NS.
ThirdAge - Adam - Noonan Syndrome
noonan syndrome. Definition noonan syndrome can be inherited in an autosomal dominant manner. It affects at least 1 in 2,500 children.
http://www.thirdage.com/health/adam/ency/article/001656.htm

Extractions: Activities Games Health Horoscopes ... 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. 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.
EPEC - Educating Parents Of Extra-special Children - Noonan Syndrome
noonan syndrome. noonan syndrome is a rare genetic disorder that is typically evident at birth (congenital). The noonan syndrome Support Group, Inc.
http://www.epeconline.com/NS.html
WebRing: Hub
Conditions and Diseases noonan syndrome Top Links noonan syndrome Web Site Links. The noonan syndrome Support Group - Information about this organization as well the disease itself.
http://www.webring.org/cgi-bin/webring?home&ring=noonan
Genetic Disorders: Noonan Syndrome
Genetic Disorders noonan syndrome. Birth Defects Foundation noonan syndrome. eMedicine noonan syndrome Article by Jennifer Ibrahim, MD.
http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/No

Extractions: Home Health Conditions and Diseases Genetic Disorders : Noonan Syndrome google_ad_client = 'pub-3272565765518472';google_ad_width = 336;google_ad_height = 280;google_ad_format = '336x280_as';google_color_border = 'FFFFFF';google_color_bg = 'FFFFFF';google_ad_channel ='7485447737';google_alternate_color = 'FFFFFF';google_color_link = '0000FF';google_color_url = '008000';google_color_text = '000000';
Noonan Syndrome
PTPN11 Gene Test for noonan syndrome. Clinical Features *Features in bold are the most common manifestations of noonan syndrome. Growth. ? Short stature.
http://www.hpcgg.org/LMM/comment/Noonan Info sheet.htm

Extractions: Gene Test for Noonan Syndrome Synonyms: Noonan syndrome (Online Mendelian Inheritance in Man #163950) Gene: (protein tyrosine phosphatase non-receptor type 11, OMIM #176876) Protein: Nonreceptor protein tyrosine phosphatase SHP2 Location: Other diseases caused by mutations in the same gene: LEOPARD syndrome (OMIM #151100) Epidemiology: Both males and females are affected in equal frequency, and there is no known association with ethnic origin. Clinical Features: * Features in bold are the most common manifestations of Noonan syndrome Growth Short stature Facial Dysmorphology Epicanthal folds Ptosis of eyelids Hypertelorism Low nasal bridge Downward eye slant Hearing Hearing loss Eye Nystagmus Strabismus Neck Broad or webbed neck Heart Pulmonary valve stenosis Left ventricular hypertrophy Septal defects Patent ductus arteriosis Cognitive development Learning disability Mental retardation Bleeding diathesis Von Willebrand disease Thrombocytopenia Factor deficiencies (VII, XI, XII)
Health, Conditions And Diseases, Genetic Disorders: Noonan Syndrome
HealthConditions and DiseasesRare Disorders. Birth Defects Foundation noonan syndrome History of the Foundation s involvement with Noonan s.
http://www.combose.com/Health/Conditions_and_Diseases/Genetic_Disorders/Noonan_S

Extractions: Related links of interest: Health:Conditions and Diseases:Rare Disorders Birth Defects Foundation: Noonan Syndrome - History of the Foundation's involvement with Noonan's. Printable booklet and newsletter. NORD - Noonan Syndrome - Offers the synonyms, a general discussion and further resources. National Library of Medicine - Includes the alternate names, a summary and a list of major features for Noonan syndrome. Noonan Syndrome - by Michelle Ellis - Account of her life with the disorder. Noonan Syndrome - Story of 6-year-old Becky, with factsheet and resources. Pediatric Database - A definition of Noonam syndrome, the epidemiology, pathogenesis, clinical features, investigations and management. The CaF Directory - A description of Noonan syndrome, its inheritance patterns and pre-natal diagnosing. The Noonan Syndrome Support Group - Information about this organization as well the disease itself. Offers news, events, a survey, a newsletter and further resources. eMedicine - Noonan Syndrome : Article by Jennifer Ibrahim, MD

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