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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

21. Apert Syndrome Definition From Answers.com
n.pr Craniostenosis characterized by oxycephaly and syndactyly of the hands and feet. Facial manifestations include exophthalmos, high prominent forehead, small nose, and
http://www.answers.com/topic/type-i-acrocephalosyndactyly

22. Apert Syndrome Answerbag
Apert Syndrome. Learn about Apert Syndrome on Answerbag.com. Get information and videos on Apert Syndrome including articles on asherman syndrome, aase syndrome, bassen
http://www.answerbag.com/apert-syndrome

23. CCDD Apert Syndrome
The Center for Craniofacial Development and Disorders at Johns Hopkins University, provides information on this disorder, its causes, diagnosis and treatment.
http://www.hopkinsmedicine.org/craniofacial/Education/Article.cfm?ArticleID=1&So

24. Apert Syndrome MedlinePlus Medical Encyclopedia
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. Causes
http://www.nlm.nih.gov/medlineplus/ency/article/001581.htm

25. Apert Syndrome
Apert syndrome, also known as acrocephalosyndactyly type 1 (ACS1), is a rare genetic disorder that occurs when the bones in the skull fuse together sooner than normal. This
http://www.wellness.com/reference/conditions/apert-syndrome/prevention-and-treat

26. CCDD Apert Syndrome
Information for physicians including clinical manifestations, genetics, pathophysiology, diagnosis and treatment.
http://www.hopkinsmedicine.org/craniofacial/Education/Article.cfm?ArticleID=1&So

27. Apert Syndrome - What Is Apert Syndrome
Information about Apert syndrome including its symptoms, diagnosis, and treatment.
http://rarediseases.about.com/cs/musclesbonesjoints/a/040503.htm

28. Apert Syndrome
A US Department of Health and Human Service project providing information on genetic and rare diseases. A comprehensive body of resources on Apert syndrome
http://rarediseases.info.nih.gov/GARD/Disease.aspx?PageID=4&diseaseID=5833

29. Apert
a guide to understanding apert syndrome t his parent's guide to Apert syndrome is designed to answer questions that are frequently asked by parents of a child with Apert syndrome.
http://www.ccakids.com/Syndrome/Apert.PDF

30. Apert Syndrome Information On Healthline
Premature closure of the skull bones leading to facial distortion with an unusually tall skull and fusion of the fingers and toes, known as syndactyly, are the major features of
http://www.healthline.com/galecontent/apert-syndrome-1

31. Krista S Page
Written by her father, this contains biographical detail about living with Apert syndrome.
http://www.apert.org/horning/index.htm

32. Apert Syndrome Seattle Children's Hospital
Apert syndrome is caused by early fusion of one or more sutures in the skull. Children with Apert syndrome have head, face, hand and feet abnormalities.
http://www.seattlechildrens.org/medical-conditions/chromosomal-genetic-condition

33. Contact A Family Apert Syndrome
UK charity for families with disabled children provides information on this rare disorder, its symptoms, causes, how it is diagnosed and treated, inheritance patterns and prenatal diagnosis.
http://www.cafamily.org.uk/medicalinformation/conditions/azlistings/a635.html

34. APERT SYNDROME - OMIM Result
OMIM, Online Mendelian Inheritance in Man, a database of human genes and genetic disorders developed by staff at Johns Hopkins and hosted on the Web by NCBI.
http://www.ncbi.nlm.nih.gov/omim/101200

35. Older Dad Baby Defect Explained
BBC story on the discovery that children born of older fathers are at greater risk of developing Apert, and the mechanism behind that risk.
http://news.bbc.co.uk/1/hi/health/3114789.stm

36. Apert Syndrome - My Child Has - Children's Hospital Boston
What is Apert syndrome? Apert syndrome is a rare genetic birth disorder involving abnormal growth of the skull and the face, as well as fused fingers and toes.
http://www.childrenshospital.org/az/Site789/mainpageS789P0.html

37. Elterninitiative Apert-Syndrom Und Verwandte Fehlbildungen E.V.
Die Initiative pr sentiert sich und ihre Schwerpunkte. Sie bietet Wissenswertes zu den Syndromen, Veranstaltungen, Referate sowie ein Forum und Chat zum Austausch.
http://www.apert-syndrom.de/

38. Att Leva Med Apert Syndrome Som Barn Och Vuxen
Om ansiktsmissbildning.
http://apert.org/sweden/

39. Apert Syndrome
National Organization for Rare Disorders is dedicated to helping people with rare, orphan diseases. Rarediseases.org contains information on the prevention, treatment and cure
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Apert Syndrom

40. Florida - Space Coast Early Intervention Center
A nationally recognized not-for-profit pre-school and therapeutic center for families and children with Down syndrome, William s syndrome, Rett syndrome, Cerebral palsy, Autism, P-4 Deletion syndrome, PDD and Apert syndrome.
http://www.sceic.com/

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