1. NORD - National Organization For Rare Disorders, Inc. National Organization for Rare Disorders is dedicated to helping people withrare, orphan diseases. Rarediseases.org contains information on the prevention, http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Craniofronton

2. OMIM National Center For Biotechnology Information A clinical synopsis of craniofrontonasal dysplasia. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

3. Craniofrontonasal Dysplasia - St. Joseph Mercy, Ann Arbor Michigan craniofrontonasal dysplasia St. Joseph Mercy Health System Hospitals servingAnn Arbor, SE Michigan, Washtenaw County, Livingston County, Wayne County, http://www.sjmercyhealth.org/13265.cfm

@import url(default.css); Online Health Information Health Information - Rare Diseases and Disorders Back to Health Library Print This Page Email to a Friend National Organization for Rare Disorders, Inc. Craniofrontonasal Dysplasia Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Craniofrontonasal Dysplasia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms CFND Craniofrontonasal Dysostosis Craniofrontonasal Syndrome Disorder Subdivisions None General Discussion Craniofrontonasal dysplasia is a very rare inherited disorder characterized by abnormalities of the head and face (craniofacial area), hands and feet, and certain skeletal bones. Major symptoms of this disorder may include widely spaced eyes (ocular hypertelorism), a groove (cleft) on the tip of the nose, an unusually wide mouth, malformations of the fingers and toes, and/or underdevelopment of portions of the face (midface hypoplasia), such as the forehead, nose, and chin. In addition, the head may have an unusual shape due to premature closure of the fibrous joints (sutures) between certain bones in the skull (coronal synostosis). Craniofrontonasal dysplasia follows X-linked inheritance in most families, but females are more severely affected than males. An autosomal dominant form of the disorder has also been discussed in the medical literature.

4. Redirect A clinical synopsis of craniofrontonasal dysplasia. http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?304110

5. Craniofrontonasal Syndrome (CNFS) View the Full Record. Syndrome craniofrontonasal syndrome (CNFS) Synonyms craniofrontonasal dysostosis craniofrontonasal dysplasia (CFND) http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

6. Craniofrontonasal Dysplasia craniofrontonasal dysplasia is a very rare inherited disorder characterized byabnormalities of the http://webcenter.health.webmd.netscape.com/hw/brain_nervous_system/nord1049.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Craniofrontonasal Dysplasia Important It is possible that the main title of the report Craniofrontonasal Dysplasia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms CFND Craniofrontonasal Dysostosis Craniofrontonasal Syndrome Disorder Subdivisions None General Discussion Craniofrontonasal dysplasia is a very rare inherited disorder characterized by abnormalities of the head and face (craniofacial area), hands and feet, and certain skeletal bones. Major symptoms of this disorder may include widely spaced eyes (ocular hypertelorism), a groove (cleft) on the tip of the nose, an unusually wide mouth, malformations of the fingers and toes, and/or underdevelopment of portions of the face (midface hypoplasia), such as the forehead, nose, and chin. In addition, the head may have an unusual shape due to premature closure of the fibrous joints (sutures) between certain bones in the skull (coronal synostosis). Craniofrontonasal dysplasia follows X-linked inheritance in most families, but females are more severely affected than males. An autosomal dominant form of the disorder has also been discussed in the medical literature.

7. Craniofrontonasal Dysplasia - Quest Diagnostics Patient Health craniofrontonasal dysplasia is a very rare inherited disorder characterized by abnormalities of the head and face (craniofacial area), hands and http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

8. Craniofrontonasal Dysplasia craniofrontonasal dysplasia is a very rare inherited disorder characterized byabnormalities of the head and face (craniofacial area), hands and feet, http://www.bchealthguide.org/kbase/nord/nord1049.htm

var hwPrint=1;var hwDocHWID="nord1049";var hwDocTitle="Craniofrontonasal Dysplasia";var hwRank="1";var hwSectionHWID="nord1049-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. Craniofrontonasal Dysplasia Important It is possible that the main title of the report Craniofrontonasal Dysplasia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms CFND Craniofrontonasal Dysostosis Craniofrontonasal Syndrome Disorder Subdivisions None General Discussion Craniofrontonasal dysplasia is a very rare inherited disorder characterized by abnormalities of the head and face (craniofacial area), hands and feet, and certain skeletal bones. Major symptoms of this disorder may include widely spaced eyes (ocular hypertelorism), a groove (cleft) on the tip of the nose, an unusually wide mouth, malformations of the fingers and toes, and/or underdevelopment of portions of the face (midface hypoplasia), such as the forehead, nose, and chin. In addition, the head may have an unusual shape due to premature closure of the fibrous joints (sutures) between certain bones in the skull (coronal synostosis). Craniofrontonasal dysplasia follows X-linked inheritance in most families, but females are more severely affected than males. An autosomal dominant form of the disorder has also been discussed in the medical literature. Resources Children's Craniofacial Association

9. Craniofrontonasal Dysplasia craniofrontonasal dysplasia Abnormalities of the head and face, hands and feet and skeletal bones typify this rare, inherited disorder. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

10. Orocraniodigital Syndrome craniofrontonasal dysplasia is a rare inherited disorder characterized by craniofrontonasal dysplasia is thought to be inherited as an autosomal http://www.bchealthguide.org/kbase/nord/nord1048.htm

var hwPrint=1;var hwDocHWID="nord1048";var hwDocTitle="Orocraniodigital Syndrome";var hwRank="1";var hwSectionHWID="nord1048-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. Orocraniodigital Syndrome Important It is possible that the main title of the report Orocraniodigital Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Juberg Hayward Syndrome Cleft Lip/Palate with Abnormal Thumbs and Microcephaly Cranio-Oro-Digital Syndrome Digital-Oro-Cranio Syndrome Disorder Subdivisions None General Discussion Orocraniodigital syndrome is an extremely rare inherited disorder characterized by multiple malformations of the head and face (craniofacial area) and the fingers and toes (digits). Major characteristics may include a vertical groove in the upper lip (cleft lip) and/or the inside, upper portion of the mouth (cleft palate), an abnormally small head (microcephaly), widely spaced eyes (ocular hypertelorism), improper development (hypoplasia) of the thumbs and/or toes, and/or webbing (syndactyly) of the toes. In some cases, malformations of certain skeletal bones may also be present. Mental retardation has occurred in the majority of cases. Orocraniodigital syndrome may be inherited as an autosomal recessive genetic trait. Resources Children's Craniofacial Association 13140 Coit Road Suite 307 Dallas, TX 75240

11. CRANIOFRONTONASAL DYSPLASIA Features Listed For craniofrontonasal dysplasia McKusick 304110. Abnormal auditory ossicles Bifid nasal tip Brachycephaly Broad http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

12. Craniofrontonasal Dysplasia Synonyms, Eastern Carolina craniofrontonasal dysplasia Synonyms University Health Systems of EasternCarolina serves tarboro, ahoskie, edento, winsor, maxhead, dear county, http://www.uhseast.com/112523.cfm

Health News Health Library Health Topics Healthy Living ... Nutrition Information on diseases and health concerns, including symptoms, treatment options, and prevention. Craniofrontonasal Dysplasia Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Craniofrontonasal Dysplasia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms CFND Craniofrontonasal Dysostosis Craniofrontonasal Syndrome Disorder Subdivisions None General Discussion Craniofrontonasal dysplasia is a very rare inherited disorder characterized by abnormalities of the head and face (craniofacial area), hands and feet, and certain skeletal bones. Major symptoms of this disorder may include widely spaced eyes (ocular hypertelorism), a groove (cleft) on the tip of the nose, an unusually wide mouth, malformations of the fingers and toes, and/or underdevelopment of portions of the face (midface hypoplasia), such as the forehead, nose, and chin. In addition, the head may have an unusual shape due to premature closure of the fibrous joints (sutures) between certain bones in the skull (coronal synostosis). Craniofrontonasal dysplasia follows X-linked inheritance in most families, but females are more severely affected than males. An autosomal dominant form of the disorder has also been discussed in the medical literature. Resources Children's Craniofacial Association

13. Craniofrontonasal Dysplasia craniofrontonasal dysplasia Direct access to data Clinical signs. Bifid tip/cleft nose Brachycephaly/plat occiput Broad nose http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

14. Craniofrontonasal Dysplasia craniofrontonasal dysplasia. Abnormalities of the head and face, hands and feetand skeletal bones typify this rare, inherited disorder. http://www.forwardface.org/misc_text/conditions/craniofront.htm

Craniofrontonasal Dysplasia Abnormalities of the head and face, hands and feet and skeletal bones typify this rare, inherited disorder. Noticeable symptoms include: a groove (cleft) on the tip of the nose, an unusually wide mouth and widely spaced eyes (ocular hypertelorism), malformations of toes and fingers and underdeveloped mid-face (forehead, nose, chin). The shape of the head is unusually wide and short. Other possible characteristics of this condition are: diminished muscle tone, developmental delays, hearing loss, and sunken or protruding posturing of certain body areas.

15. Health Disorders And Diseases Genetic Disorders/Craniofrontonasal the entire directory only this category More search options. Home Genetic Disorders craniofrontonasal dysplasia LINKS http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

16. Health/Conditions And Diseases/Genetic Disorders/Craniofrontonasal Dysplasia -- NORD craniofrontonasal dysplasia Offers a general discussion and resources. A clinical synopsis of craniofrontonasal dysplasia. http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Genetic_Disor

Advertisement Powered by Careerbuilder Search for: Home Humor Advertising Contact ... Links Specialties Cardiology Chest diseases Dermatology Endocrinology ... Urology Other Sections Membership Research Tools Medical Tutorials Medical Software ... Specialized Centers Headlines: The Medical Website Directory Popular Categories Popular Links Web Sites National Library of Medicine: CNFS Offers synonyms of craniofrontonasal syndrome, a summary and a list of features. url: www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome2... NORD: Craniofrontonasal Dysplasia Offers a general discussion and resources. url: www.rarediseases.org/search/rdbdetail_abstract.htm... OMIM: National Center for Biotechnology Information A clinical synopsis of Craniofrontonasal Dysplasia. url: www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?3041... mozilla.org url: mozilla.org/ More Search All the Web AltaVista Gigablast Google USENET ... Yahoo In association with ODP Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Are you a physician or a nurse? Would you like to join us and help patients online by volunteering even a few minutes of your time?

17. Web Resources Directory - Craniofrontonasal Dysplasia Top Health Conditions and Diseases Genetic Disorders craniofrontonasal dysplasia http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

18. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Genetic_Disorders/ Information A clinical synopsis of craniofrontonasal dysplasia. NORDcraniofrontonasal dysplasia - Offers a general discussion and resources. http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Genetic_Dis

@import "/styles/navbar.css"; @import "/styles/tabStyles.css"; Set home page Bookmark site Add search Latest News ... Email to friend Text Size A A A Front Page ... Genetic Disorders : Craniofrontonasal Dysplasia Subtopics See Also: Health: Conditions and Diseases: Rare Disorders Search Google: Craniofrontonasal Dysplasia News Books Links ... Dye Imaging ID's Oral Lesions Likely To Become Cancer (September 1, 2005) full story Study Casts Doubt On Lung Treatment For Preterm Infants (July 11, 2005) full story Researchers Trace Evolution To Relatively Simple Genetic Changes (May 31, 2005) full story A Shallow Hip Socket Predicts Osteoarthritis Of The Hip (March 21, 2005) full story Mechanical Tension Helps Shape Lung Development (March 5, 2005) full story Dog Genome Yields Information That May Benefit Human Health (May 21, 2004) full story Possible Link Discovered Between Gene Responsible For Blood Vessel Development And ACD In Newborns (March 12, 2004) full story Activation Of Receptor Ups Development Of Precancerous Intestinal Polyps (February 2, 2004) full story [ More news about Craniofrontonasal Dysplasia Error: We did not find any matches for your request.

19. Analysis Of Craniofrontonasal Dysplasia Disease mapped craniofrontonasal dysplasia Chromosome X Genomic positionstartstop 1-26000000 length 26000000 Band Xp22, LINKS. LocusLink 1079 http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U1079

20. Complete List Of GO Terms Associated To Craniofrontonasal Dysplasia Complete list of GO terms associated to craniofrontonasal dysplasia, G2D Home.The number reflects their association to the disease according to the set of http://www.bork.embl-heidelberg.de/g2d/list_go_disease.pl?U1079:Craniofrontonasa

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