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Apert Syndrome: more detail | ||||||
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1. Wikipedia Apert Syndrome Encyclopedia article on this congenital disorder characterized by malformations of the skull, face, hands and feet. http://en.wikipedia.org/wiki/Apert_syndrome |
2. Apert Syndrome - Wikidoc You don't need to be EditorIn-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of http://www.wikidoc.org/index.php/Apert_syndrome |
3. Apert Syndrome Symptoms, Diagnosis, Treatments And Causes Apert syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. http://www.wrongdiagnosis.com/a/apert_syndrome/intro.htm |
4. Apert Syndrome - Hope For Kids Apert syndrome is a rare hereditary condition that affects about one in every 160,000 births. Children with Apert syndrome have premature closure of the cranial sutures http://www.hopeforkids.com/site/c.lpISKYOvFkG/b.4205009/k.997E/Apert_Syndrome.ht |
5. Apert Syndrome Ask.com Encyclopedia Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch http://www.ask.com/wiki/Apert_syndrome?qsrc=3044 |
6. Apert Syndrome - Medpedia Apert Syndrome is an inherited disorder of the bones and connective tissues that leads to a characteristic pattern of deformities in the head, hands, and feet, which http://wiki.medpedia.com/Apert_Syndrome |
7. What Is Apert Syndrome? What is Apert Syndrome? The following was developed from information contained in an article entitled Clinical Assessment and Multispecialty Management of Apert Syndrome http://www.apert.org/apert.htm |
8. Apert Syndrome What is Apert Syndrome? Apert Syndrome is a condition involving distortions of the head and face and webbing of the hands and feet. Characteristics include http://www.faces-cranio.org/Disord/Apert.htm |
9. Teeter's Page A family support network for people affected by Apert syndrome and other craniofacial disorders. http://www.apert.org/ |
10. Apert Syndrome Resource for contacts, chat rooms, pen pals and other relevant links. http://www.familyvillage.wisc.edu/lib_aprt.htm |
11. Apert Syndrome Information about Apert syndrome from the Rare Disease Database of the Swedish National Board of Health and Welfare. http://www.socialstyrelsen.se/english/rarediseases/apertsyndrome |
12. Apert Syndrome Definition - Medical Dictionary Definitions Of Online Medical Dictionary and glossary with medical definitions http://www.medterms.com/script/main/art.asp?articlekey=6575 |
13. Swedish Apert Syndrome Information General information about Apert syndrome with photographs of people with the condition. English version follows Swedish text. http://www.apert.org/sweden/index.htm |
14. Apert Syndrome - Genetics Home Reference Apert syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing normally http://ghr.nlm.nih.gov/condition=apertsyndrome |
15. Apert Syndrome Treatment Medication - EMedicine Pediatrics Treatment Apert syndrome is named for the French physician who described the syndrome acrocephalosyndactylia in 1906.Apert syndrome is a rare autosomal dominant disorder http://emedicine.medscape.com/article/941723-treatment |
16. UT Medical Center - Apert Syndrome University of Tennessee Medical Center has a rich history in the community of providing patientcentered care and remaining at the forefront of research, technology and treatments. http://www.utmedicalcenter.org/encyclopedia/1/001581.htm |
17. Apert Syndrome Symptoms And Diagnosis Seattle Children's Hospital Signs and symptoms of Apert syndrome include abnormally shaped head and face. Children with Apert syndrome typically have fused fingers and toes. http://www.seattlechildrens.org/medical-conditions/chromosomal-genetic-condition |
18. Apert Syndrome EMedicine Pediatrics Genetics And Metabolic Disease Overview Apert syndrome is named for the French physician who described the syndrome acrocephalosyndactylia in 1906.Apert syndrome is a rare autosomal dominant disorder http://emedicine.medscape.com/article/941723-overview |
19. Apert Syndrome - Scripps Health - San Diego Definition. Apert syndrome is a genetic disease in which the seams between the skull bones close earlier than normal. This affects the shape of the head and face. http://www.scripps.org/articles/2416-apert-syndrome |
20. Apert International Inc. Charitable organization set up to provide direct financial and emotional assistance to families affected by Apert Syndrome. Donations welcomed. http://www.apert-international.org/ |
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