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         Cleidocranial Dysplasia:     more detail
  1. Cleidocranial dysplasia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Jennifer, MS, CGC Roggenbuck, 2005

21. Cleidocranial Dysplasia Home
To report deadlinks or other technical problems with the site, feel free to emailthe webmaster. © Copyright 2000 cleidocranial dysplasia Foundation.
http://www.cleidocranialdysostosis.org/home.html
Welcome
Note: Because we are receiving a larger influx of forms, it may take up to a week to process membership, penpal, and messageboard submissions. For now they'll be updated irregularly throughout the week, but no later than Friday of each week. According to Mosby's Medical, Nursing, and Allied Health Dictionary (Fourth Edition), Cleidocranial Dysplasia is a rare abnormal hereditary condition characterized by defective ossification of the cranial bones and by the complete or partial absence of the clavicles. It is transmitted as an autosomal dominant trait. The defective ossification of the cranial bones delays the closing of the cranial sutures and results in large fontanels. The complete or partial absence of the clavicles allows the shoulders to be brought together. This condition also involves dental and vertebral anomalies. The Cleidocranial Dysplasia Foundation (CCDF) believes all people with cleidocranial dysostosis syndrome or cleidocranial dysplasia (CCD), in the world, should have access to three things:
  • Other people in their age group who could be an e-mail pen pal or peer counselor.

22. Cleidocranial Dysplasia Message Board
Links to other cleidocranial dysplasia sites. The links below are linksto medical Copyright 2000 cleidocranial dysplasia Foundation.
http://www.cleidocranialdysostosis.org/links.html
Links to other Cleidocranial Dysplasia sites
The links below are links to medical sites devoted to Cleidocranial Dysplasia. They are seperated into professional and non-professional catagories.

23. Cleidocranial Dysplasia
cleidocranial dysplasia. References. See related articles. SearchMedline for cleidocranial dysplasia. Related differential diagnosis.
http://www.gentili.net/list4.asp?ID=448

24. Ccd - Cleidocranial Dysplasia
Features Listed For Ccd cleidocranial dysplasia.Chromosome MOUSE GENOME DATABASE (MGD).
http://www.hgmp.mrc.ac.uk/dhmhd-bin/mous-look-up?434

25. Cleidocranial Dysplasia
cleidocranial dysplasia. 10/15/02. Click here to start. Table of Contents.cleidocranial dysplasia. cleidocranial dysplasia. Introduction. PPT Slide.
http://www.dental.mu.edu/oralpath/spresent/cleidocranial/
Cleidocranial Dysplasia
Click here to start
Table of Contents
Cleidocranial Dysplasia CLEIDOCRANIAL DYSPLASIA Introduction PPT Slide ... Special thanks to: Author: Robert V. Wolf

26. Cleidocranial Dysplasia
Next Last Index Text. Slide 1 of 19.
http://www.dental.mu.edu/oralpath/spresent/cleidocranial/sld001.htm

27. Cleidocranial Dysplasia
cleidocranial dysplasia. Examinations PhotographsMovies Links Home Search noJava Home.
http://medgen.genetics.utah.edu/photographs/pages/cleidocranial_dysplasia.htm
cleidocranial dysplasia
Examinations Photographs Movies Links ... noJava Home

28. Cleidocranial Dysplasia : Meddie Health Search
ITEMS LINKS Baylor College of Medicine An article entitled A NaturalHistory of cleidocranial dysplasia. (Rating 0.00 Votes 0
http://www.meddie.com/search/Health/Conditions_and_Diseases/Rare_Disorders/Cleid
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29. University Of Miami School Of Medicine - Glossary - Cleidocranial Dysplasia
cleidocranial dysplasia. What is cleidocranial dysplasia? POWER POINTS Cleidocranialdysplasia (CCD) is a bone disorder which is present from birth.
http://www.med.miami.edu/patients/glossary/art.asp?articlekey=7913

30. Health Library - Cleidocranial Dysplasia
cleidocranial dysplasia. None. General Discussion. cleidocranial dysplasiais a rare craniofacial disorder inherited as an autosomal dominant trait.
http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

31. Wheeless' Textbook Of Orthopaedics
cleidocranial dysplasia (Dysostosis);. Discussion - autosomal dominantproportionate dwarfism that affects bones formed intramembranously (eg.
http://www.ortho-u.net/o14/80.htm
Main Menu Home Page
Cleidocranial Dysplasia (Dysostosis);
- Discussion: pseurdoarthrosis of the clavicle coxa vara Medical Progress: Epiphyseal Disorders. The epiphyseal dysplasias. Sprenger J: CORR 1976;114:46. Avascular necrosis of the hip in multiple epiphyseal dysplasia. Mackenzie W et al. J Pediatr Orthop 1989;9:666-671. Development of the hip in multiple epiphyseal dysplasia. Natural history and susceptibility to premature osteoarthritis.

32. Wheeless' Textbook Of Orthopaedics
Deformities of the Limbs Achondroplasia Chondrodysplasia Punctata ChondroectodermalDysplasia cleidocranial dysplasia Diastrophic Dwarfism Hypophosphatemic
http://www.ortho-u.net/o14/91.htm
Main Menu Home Page
Dwarfism and Dysplasias:
Deformities of the Limbs Achondroplasia Chondrodysplasia Punctata: Chondroectodermal Dysplasia ... Spondyloepiphyseal Dysplasia Congenita - Short Trunk Dwarfism: Kniest syndrome Metatrophic Dysplasia Spondyloepiphyseal dysplasias - Proportionate Dwarism: diastrophic dysplasia cleidocranial dysplasia dysplasia - mucopolysaccaridoses - Disproportionate dwarfism: (short limb dysplasia) Achondroplasia metaphyseal chondrodysplasias - Misc: - Rhizomelic Dwarfism: Arms or Thighs are Short relative to the entire limb - Mesomelic Dwarfism: Disproportionately Short Forearms or Legs - Acromelic Dwarfism: Disproportionately short hands or feet

33. Current Features In TBASE
Cbfa1 Boneless Knockouts A Model for Human cleidocranial dysplasia. Mutationsinvolving the transcription factor CBFA1 cause cleidocranial dysplasia.
http://tbase.jax.org/docs/Cbfa1.html
Current Features in TBASE
by Anna V. Anagnostopoulos JUNE 1997 Left to Right: Apert Syndrome, Crouzon Syndrome, Tricho-Dento-Osseous Syndrome, Cleidocranial Dysplasia , and Cleft Lip and Palate
Cbfa1 Boneless Knockouts: A Model for Human Cleidocranial Dysplasia
June 1997 features two independent reports on "boneless" mice, each describing a targeted inactivation of the murine core binding factor alpha 1 ) gene. Komori et al., demonstrate that Cbfa1-null mice ( TBASE:4471 ) are smaller and neonatally lethal due to respiratory failure, and exhibit an arrest in osteoblast development from mesenchyme and therefore no ossification. Importantly, Cbfa1 heterozygous mutants ( TBASE:4470 ) display skeletal abnormalities which are characteristic of the human dominantly inherited skeletal disorder known as cleidocranial dysplasia (CCD) . These include hypoplastic clavicles and nasal bones as well as retarded ossification of the parietal, interparietal, and supraoccipital bones. Similar findings are concurrently published in Cell TBASE:4472 TBASE:4473 ) by Otto et al., 1997

34. Health Library - Cleidocranial Dysplasia
cleidocranial dysplasia. None. General Discussion. cleidocranial dysplasiais a rare craniofacial disorder inherited as an autosomal dominant trait.
http://www.laurushealth.com/library/healthguide/illnessconditions/topic.asp?hwid

35. Cleidocranial Dysplasia Family
cleidocranial dysplasia family. Follow Thanks to the Web, I could finallyhave some clear information about cleidocranial dysplasia. I
http://marge.com/bboard/messages/1377.html
Cleidocranial dysplasia family
Follow Ups Post Followup Hypermobile Joints Forum Posted by Jean-Pierre COHEN on November 20, 1999 at 13:03:16: Thanks to the Web, I could finally have some clear information about cleidocranial dysplasia.
I am a man, 43 year old, with 3 children, one boy (14) and 2 daughters (12 and 10).
The boy and the youngest daughter are both affected with the same disease.
The symptoms are classical:
One other “exotic” symptom is :
I suffered quite a lot in order to be able to eat normally, until I decided to have a dental prosthesis ... big and expensive... A couple of years ago this disease was not really well known in Europe.
I would like to avoid these problems for my children.
Does somebody know about a therapy or anything that can avoid big surgical operation?
Where can we find any forum, links ..etc ?
We are living in belgium and would like to have some correspondence with some other happy members of the club...
We speak and write French, English, Portuguese. We read Spanish, Italian. Thanks in advance.

36. Re: Cleidocranial Dysplasia Family
Re cleidocranial dysplasia family. In Reply to Re cleidocranial dysplasiafamily posted by Joanne Drinkwater on May 01, 2000 at 183112
http://marge.com/bboard/messages/2770.html
Re: Cleidocranial dysplasia family
Follow Ups Post Followup Hypermobile Joints Forum Posted by Mikko Halsas on May 08, 2000 at 03:54:31: In Reply to: Re: Cleidocranial dysplasia family posted by Joanne Drinkwater on May 01, 2000 at 18:31:12: I have a daughter (4 years old), who has CCD. My two other kids, son (5) and daughter (2), do not have CCD. It has been difficult to find information about the effects of CCD to the fife of the children. So far the effects have not been too dramatic, but things like delayed closure of the anterior fontanelle, problems with teeth and inarticulate speech are difficult enough. I am interested in sharing the experiences and especially in finding Finnish families to discuss with.
Follow Ups:

37. Trefwoord: Cleidocranial Dysplasia
cleidocranial dysplasia-. Landelijke Patiënten- en Ouderverenigingvoor Schedel- en Aangezichtsafwijkingen
http://www.npcf.nl/patientenorg/gids/index/5575.htm
-cleidocranial dysplasia-
Landelijke Patiënten- en Oudervereniging voor Schedel- en Aangezichtsafwijkingen

38. 1Up Health > Health Links Directory > Conditions And Diseases: Rare Disorders: C
Sites. Baylor College of Medicine An article entitled A Natural Historyof cleidocranial dysplasia. cleidocranial dysplasia Contains
http://www.1uphealth.com/links/rare-disorders-cleidocranial-dysplasia.html
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Sites Baylor College of Medicine An article entitled: A Natural History of Cleidocranial Dysplasia. Cleidocranial Dysplasia Contains information about this rare genetic disorder, chat and more topics for discussion. Cleidocranial Dysplasia Find information about this rare genetic disorder, chat and more topics for discussion. MedicineNet.com: Medical Dictionary An explanation of what cleidocranial dysplasia is and how it is transmitted. National Library of Medicine: CCD, CLCD A list of synonyms of sleidocranial dysplasia, along with a summary and major features. Readers Digest Health Cleidocranial dysplasia, a list of alternate names, a general discussion and further resources.

39. 1Up Health > Cleidocranial Dysostosis (Cleidocranial Dysplasia) Information
Comprehesive information on Cleidocranial dysostosis (cleidocranial dysplasia). Guide.Alternative names cleidocranial dysplasia. Definition
http://www.1uphealth.com/health/cleidocranial_dysostosis.html
1Up Health Alternative Medicine Clinical Trials Health News ... Health Topics A-Z Search 1Up Health Cleidocranial dysostosis Information Guide Alternative names : Cleidocranial dysplasia Definition : An autosomal dominant inherited disorder of bony development characterized by absent or incompletely formed collar bones, characteristic facial appearance, short stature, and dental abnormalities.
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Causes, Incidence, and Risk Factors

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40. Page Not Found
cleidocranial dysplasia. Syndrome, cleidocranial dysplasia. Gene Name,Corebinding factor, runt domain, alpha subunit 1. Gene Symbol, CBFA1.
http://www.nidr.nih.gov/cranio/detail/119600.htm
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