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Apert Syndrome: more detail

Apert Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-08-31
Apert syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Suzanne, MS, CGC Carter, 2005
Physical activity for children with Apert syndrome.: An article from: Palaestra by Robert C. Weber, 1994-01-01
Dysostoses: Syndrome D'apert, Syndrome de Rubinstein-Taybi, Syndrome Oro-Facio-Digital Type 1, Syndrome de Greig, Syndrome de Pfeiffer (French Edition)
Apert Syndrome
Apert Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19

lists with details

CCDD: Physician: Education: Descriptions Of Disorders: Apert Syndrome
Within the spectrum of craniosynostosis disorders caused by mutations in the fibroblast growth factor receptor genes, apert syndrome is somewhat unique.
http://www.hopkinsmedicine.org/craniofacial/Education/Article.cfm?ArticleID=1&So
Medical Encyclopedia
Back to main Health Information page Disease apert syndrome. treatment. Definition apert syndrome is a genetic disease. It can
http://www.georgetownuniversityhospital.org/body.cfm?id=18&action=Display&articl
University Of Miami School Of Medicine - Glossary - Apert Syndrome Acrocephalosy
apert syndrome acrocephalosyndactyly. apert syndrome acrocephalosyndactyly An inherited disorder causing abnormalities of the skull, face and hands and feet.
http://www.med.miami.edu/patients/glossary/art.asp?articlekey=6605
University Of Miami School Of Medicine - Glossary - Apert Syndrome
Medical Dictionary. apert syndrome. Apert Moreover, the mutation that causes apert syndrome affords the sperm a selective advantage. The
http://www.med.miami.edu/patients/glossary/art.asp?articlekey=6575
Apert Syndrome
apert syndrome. (See also CRANIOFACIAL DISORDERS);. Apert Support and Information Network,. (415) 3611095 (voice/fax). apert syndrome Pen Pal Network,. PO Box 115.
http://www.childhealthinfo.com/apert-syndrome.htm

Extractions: APERT SYNDROME (See also CRANIOFACIAL DISORDERS); Apert Support and Information Network, 1626 Redwood Ave Redwood City, CA 94061 (415) 361-1095 (voice/fax) Apert Syndrome Pen Pal Network, PO Box 115 Providence, RI 02901 Apert Syndrome Support Group, 8708 Kathy St St. Louis, MO 63126 [Home] [Printed Guide] [Child Care for the '90's] [Links] ... MoreInfo@ChildHealthInfo.com
APERT SYNDROME
. Prevalence/Causes. apert syndrome occurs in approximately 1160,000 live births. It is caused by a genetic mutation (change).apert syndrome.
http://www.forwardface.org/misc_text/conditions/aperts.htm

Extractions: APERT SYNDROME Description Apert Syndrome, first described in 1906 by E. Apert, a French physician, is characterized by malformations (abnormal growth) of the skull and face accompanied by fusion (webbing) of the fingers and toes. The shape of the head appears long and pointed at the top. Wide-set, bulging eyes that tilt down at the sides, a sunken-in looking mid face (middle of eye socket to upper jaw) and dental crowding are often found. Skulls of newborns are comprised of sutures or plates that are loosely connected and eventually join together to form the skull. This fusion (craniosynostosis) can cause increased pressure on the brain as it develops causing the head to grow upwards. Visual problems due to eye muscle imbalance Hearing loss due to frequent infections Severe acne Mild mental retardation Cleft palate Hyperactive sweat glands Prevalence/Causes Apert syndrome occurs in approximately 1:160,000 live births. It is caused by a genetic mutation (change). Neither parent is responsible for this mutation first occurring in a family line.
A To Z Encyclopedia Topic: Apert Syndrome
Craniofacial Anomalies Programs. Unfortunately, at this time, we are not able to provide information about this condition or procedure.
http://web1.tch.harvard.edu/cfapps/A2ZtopicDisplay.cfm?Topic=Apert Syndrome
OMIM - APERT SYNDROME
http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101200
:: Ez2Find :: Apert Syndrome
Guide apert syndrome, Global Metasearch Any Language Guides, apert syndrome. ez2Find Home Directory Health Support
http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Support_Groups/Condit

Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Apert Syndrome Web Sites Andrew's Journey with Apert's [Site Info] [Translate] [Open New Window] Apert Syndrome [Site Info] [Translate] [Open New Window] Produced by Alliance of Genetic Support, this includes comprehensive information about the condition, an Apert listserve, newsgroup, links, webring and family homepages. URL: http://members.tripod.com/~bears_4/aperts.html
You Ll Find Hundreds Of Files On Cleft Lip, Cleft Palate Here On
This one is about What is apert syndrome? (c) 1997 Wide Smiles Email widesmiles@aol.com What is apert syndrome? The following was developed
http://www.widesmiles.org/cleftlinks/WS-646.html

Extractions: The following was developed from information contained in an article entitled Clinical Assessment and Multispecialty Management of Apert Syndrome, written by Lawrence C. Kaplan, MD, and published in Clinics in Plastic Surgery-Vol. 18, No. 2, April 1991. Major Features of Apert Syndrome Possible Related Features of Apert Syndrome These have been observed in some cases of Apert syndrome, although whether they were caused by Apert syndrome is uncertain. Definition Apert Syndrome is a genetic defect and falls under the broad classification of craniofacial/limb anomalies. It can be inherited from a parent who has Apert, or may be a fresh mutation. It occurs in approximately 1 per 160,000 to 200,000 live births. Apert syndrome is primarily characterized by specific malformations of the skull, midface, hands, and feet. The skull is prematurely fused and unable to grow normally; the midface (that area of the face from the middle of the eye socket to the upper jaw) appears retruded or sunken; and the fingers and toes are fused together in varying degrees. Apert syndrome is named for the French physician who first described it, E. Apert, in 1906.
What Is Apert Syndrome?
What is apert syndrome? What is apert syndrome? Individuals with apert syndrome have a 1 in 2 (50%) chance of passing this condition to their child.
http://mick.murraystate.edu/cdi684/cdi684001/ACARTER/page2.htm
Apert Syndrome
apert syndrome. This page is devoted to apert syndrome. I hope you find the information and related links helpful in your search.
http://mick.murraystate.edu/cdi684/cdi684001/ACARTER/
Apert Syndrome
Links Health Support Groups Conditions and Diseases Facial Differences apert syndrome. apert syndrome Web Search Results Below (Add Your Site or modify).
http://www.zookle.com/Health/Support_Groups/Conditions_and_Diseases/Facial_Diffe
Apert Syndrome
Directory, Home Health Support Groups Conditions and Diseases Facial Differences apert syndrome (9) See Also What is apert syndrome?
http://www.thenewhealthfind.com/Health/SupportGroups/ConditionsandDiseases/Facia

Extractions: See Also: Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Rare Disorders Teeter's Page - Teeter's story, and Teeter's Internet friends. What is Apert Syndrome? - Medical information including definition, major and related features of the condition, genetics. TJ's Journal - About Apert Syndrome and how it has affected the life of a baby boy named TJ and his family. Swedish Apert Syndrome Information - General information about Apert syndrome with photographs of people with the condition. English version follows Swedish text. Krista's Page - Written by her father, this contains biographical detail about living with Apert syndrome. Apert Syndrome - Produced by Alliance of Genetic Support, this includes comprehensive information about the condition, an Apert listserve, newsgroup, links, webring and family homepages. Apert Syndrome - Resource for contacts, chat rooms, pen pals and other relevant links. Andrew's Journey with Apert's - Written by father of child with Apert syndrome. Contains biographical detail, and links to Apert syndrome stories and support sites.
Images In Medicine: Apert Syndrome. Hosalkar HS, Shah H, Gujar P, Chaudhari A J
Year 2000 Volume 46 Issue 2 Page 129. Images in medicine apert syndrome. Images in medicine apert syndrome. J Postgrad Med 2000;46129129.
http://www.jpgmonline.com/article.asp?issn=0022-3859;year=2000;volume=46;issue=2
Medical Encyclopedia
BACK, Back to main Health Information page Disease apert syndrome. treatment. Definition apert syndrome is a genetic disease. It
http://www.medstarhealth.org/body.cfm?id=124&action=Display&articlenum=1581
Apert Syndrome
apert syndrome REASONS FOR REFERRAL To determine whether apert syndrome is responsible for abnormalities in the skull, hands, feet, or eyes.
http://genetics.hillcrest.com/apert_syndrome.htm

Extractions: Chapman Homepage Molecular Homepage Molecular Test Listing Molecular Requisition APERT SYNDROME: Apert Syndrome is generally a very distinctive and severe form of craniosynostosis, which is caused by a Pro252Arg mutation on the FGFR2 gene (chromosome 10). Apert syndrome not only features the premature closure of the sutures of the skull which can lead to mental retardation, bulging eyes and head dysmorphology, but there is generally severe hand and feet involvement. The appendages have varying degrees of syndactyly ranging from the fusion of several fingers and toes to a flipper like appearance. The prognosis is very poor. The severity of the mutation almost always is a result of a spontaneous mutation in the child. The mutation that causes this phenotype is located at a flexure point between the second and third receptor-loop structures of the extracellular end of the receptor. This is the analogous location of the mild Pfeiffer causing mutation on FGFR1 and the nonsyndromic mutation on FGFR3. This test is performed as part of the Craniosynostosis Syndromes REASONS FOR REFERRAL: To determine whether Apert syndrome is responsible for abnormalities in the skull, hands, feet, or eyes.
Health Encyclopedia
apert syndrome is a genetic disease. It can be inherited or it may occur without a known family history. It is characterized apert syndrome
http://healthcontent.baptistnortheast.com/adamcontent/ency/article/001581.asp

Extractions: Overview Symptoms Treatment ... Prevention Acrocephalosyndactyly Apert syndrome is a genetic disease. It can be inherited or it may occur without a known family history. It is characterized by premature closure of the seams between the skull bones, which results in a peaked head and an unusual facial appearance. Apert syndrome is transmitted as an autosomal dominant trait (which means that only one parent needs to have the condition for a child to potentially be affected). Some cases also appear spontaneously without a family history. The condition is caused by mutations in a gene called fibroblast growth factor receptor 2. This mutation causes some of the bony sutures of the skull close prematurely (a process called craniosynostosis) which can cause asymmetric growth and give the head a distorted shape. The face is distinctive looking and there may be full-length webbing or fusion between the 2nd, 3rd and 4th fingers, as well as the toes. In addition, as the child grows, the bones in the hands and feet become progressively fused, which reduces flexibility and function.
APERT SYNDROME - Site Map - UK Shopping Directory - UK Shops
apert syndrome Site Map UK Shopping Online, Thousands of Brand Name Products at Great Prices at UK Shops Secure UK Shops. apert syndrome.
http://www.ishop.co.uk/site-map/ap/apert_syndrome/index.shtml

Extractions: Please click here to return to the main site map index. Shopping online for apert syndrome or just looking for more information about apert syndrome? Here at www.ishop.co.uk we aim to provide the most comprehensive resource of sites selling apert syndrome and links to online resources such as search, information and price comparison tools that should quickly ensure you find sites containing information about apert syndrome or directly selling apert syndrome or releted products/services. Whilst we do not sell apert syndrome directly the independent shopping and information links provided will ensure that you find the web sites that do sell apert syndrome quickly, simply and at the best prices available ensuring you get the best deals online.
Health Library -
apert syndrome. apert syndrome, also known as acrocephalosyndactyly type I (ACS1), is a rare genetic disorder that is apparent at birth (congenital).
http://12.42.224.152/Library/HealthGuide/IllnessConditions/topic.asp?hwid=nord25

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