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

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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