1. NORD - National Organization For Rare Disorders, Inc. craniofrontonasal dysplasia. To purchase fulltext report ($7.50) Copyright1996, 2003 Synonyms of craniofrontonasal dysplasia No synonyms found. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Craniofronton

2. Result Of Search Features Listed For craniofrontonasal dysplasia. McKusick 304110. Abnormal auditory ossicles. Bifid nasal tip. Brachycephaly. Broad hallux. Camptodactyly. Camptodactyly/hammer toes. Cleft palate. Cleft upper lip (nonmidline) Clefting of nose http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?375

3. Conditions And Diseases - Craniofrontonasal Dysplasia Top Links Related Healthcare Subjects. Disabilities, Environmental Health, Fitness, Health Insurance, Healthcare Industry, Medicine, Men's Health. craniofrontonasal dysplasia Web Site Links. NORD craniofrontonasal dysplasia - NORD - craniofrontonasal dysplasia - Offers alternate names, a general discussion and resources A clinical synopsis of craniofrontonasal dysplasia. Other Useful Health Web Links http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso

Sub Categories Related Healthcare Subjects Disabilities Environmental Health Fitness Health Insurance ... Men's Health Craniofrontonasal Dysplasia Web Site Links NORD - Craniofrontonasal Dysplasia Offers alternate names, a general discussion and resources. National Library of Medicine: CNFS Offers synonyms of craniofrontonasal syndrome, a summary and a list of features. OMIM: National Center for Biotechnology Information A clinical synopsis of Craniofrontonasal Dysplasia. Other Useful Health Web Links National Institutes of Health (NIH) US Government department in charge of medical research. AHRQ: Clinical Information Clinical information on evidence-based practice, clinical guidelines, medical effectiveness, pharmaceutical therapy, new technology, screening and preventive services, outcomes research, and the National Guideline Clearinghouse. The UK Health Technology Assessment Programme Site contains details of program's many projects and publications; an NHS national research and development initiative. U.S. Preventive Services Task Force (USPSTF) Panel of health care experts that evaluates the latest scientific evidence on clinical preventive services. Controlled Trials from History A historical examination of research methods designed to reduce biases in studies assessing the effects of health care, social care and education. Contains many images of historical items.

4. Craniofrontonasal Dysplasia,CFND,Craniofrontonasal Dysostosis,Frontonasal Dyspla craniofrontonasal dysplasia CFND Craniofrontonasal Dysostosis Frontonasal Dysplasia with Coronal Craniosynostosis craniofrontonasal dysplasia CFND Craniofrontonasal Dysostosis Frontonasal Dysplasia http://www.icomm.ca/geneinfo/cfnd.htm

Craniofrontonasal Dysplasia,CFND,Craniofrontonasal Dysostosis,Frontonasal Dysplasia with Coronal Craniosynostosis,Craniofrontonasal Dysplasia,CFND,Craniofrontonasal Dysostosis,Frontonasal Dysplasia with Coronal Craniosynostosis For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Craniofrontonasal Dysplasia also known as: CFND Craniofrontonasal Dysostosis Frontonasal Dysplasia with Coronal Craniosynostosis (as defined by the National Organization for Rare Disorders 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 appear unusually wide and short (brachycephaly).

5. Birth Disorder Information Directory - CO-CZ craniofrontonasal dysplasia/Syndrome. craniofrontonasal dysplasia. CRANIOFRONTONASAL SYNDROME; CFNS. Craniofrontonasal http://www.bdid.com/defectco.htm

HOME Co-Cy COACH Syndrome See Cerebellar Vermis Hypo/Aplasia, Oligophrenia, Congenital Ataxia, Ocular Coloboma, and Hepatic Fibrosis (COACH) Syndrome Coarctation of (the) Aorta (CoA) List of Sites Coats' Disease (Congenital Retinal Telangiectasia, Exudative Retinitis, Leber Miliary Aneurysm) Coats disease Cobb Syndrome Syndromes associated with AVMs Cocaine Antenatal Infection See Fetal Cocaine Syndrome Related Books Cochin Jewish Disorder (Haim Munk Syndrome, Keratosis Palmoplantaris Periodontopathia) Keratosis palmoplantaris periodontopathia KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA AND ONYCHOGRYPOSIS Cockayne Syndrome List of Sites COD-MD Syndrome See Walker Warburg Syndrome CODAS Syndrome (Cerebrooculodentoauriculoskeletal Syndrome) Cerebro oculo dento auriculo skeletal syndrome CODAS SYNDROME Coffin Syndrome (Arthritis Short Stature Deafness) Coffin syndrome Coffin-Lowry Syndrome List of Sites Coffin Siris Syndrome (Fifth Digit Syndrome) Coffin siris syndrome FIFTH DIGIT SYNDROME COFS Syndrome See Cerebrooculofacioskeletal (COFS) Syndrome Cohen Hayden Syndrome (Proteus-Like Syndrome with Mental Retardation and Eye Defects) Cohen hayden syndrome Cohen Lockood Wyborney Syndrome (Blepharophimosis Ptosis Syndactyly Mental Retardation) blepharophimosis ptosis syndactyly mental retardation Cohen Syndrome List of Sites Colavita Kozlowski Syndrome (Short Limb Dwarf, Lethal Colavita Kozlowski Type)

6. Craniofrontonasal Syndrome (CNFS) Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes. View the Full Record. Syndrome. craniofrontonasal syndrome (CNFS) Synonyms. craniofrontonasal dysostosis. craniofrontonasal dysplasia (CFND) Summary http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome252.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome craniofrontonasal syndrome (CNFS) Synonyms craniofrontonasal dysostosis craniofrontonasal dysplasia (CFND) Summary Fontonasal dysplasia, coronal craniosynostosis, grooved nails, mild mental deficiency, and various skeletal and soft tissue abnormalities. Major Features Head and neck: Coronal suture synostosis, brachycephaly, frontal bossing, and facial asymmetry. Eyes: Soft tissue hypertelorism, increased bony interorbital distance and occasional strabismus, and downslanting palpebral fissures. Nose: Bifid nose with broad tip. Mouth and oral structures: Highly arched palate, cleft lip and/or palate, and malocclusion. Neck: Webbed. Thorax: Pectus excavatum. Abdomen: Diaphragmatic hernia. Hand and foot: Broad first toe, short first fingers, brachydactyly, clinodactyly, and gaps between the first and second toes, long fingers and toes. Transverse palmar crease is the main dermatoglyphic defect. Extremities: Sprengel shoulder, narrow sloping shoulders, hyperextensible joints Spine: Scoliosis.

7. Craniofrontonasal Dysplasia - Information / Diagnosis / Treatment / Prevention home genetic disorders craniofrontonasal dysplasia CraniofrontonasalDysplasia. Information • Diagnosis • Treatment • Prevention. http://www.healthcyclopedia.com/genetic-disorders/craniofrontonasal-dysplasia.ht

Home Health cyclopedia All Topics by Category The Good Health Search Engine Health Conditions A-Z Gurus ... genetic disorders > craniofrontonasal dysplasia Craniofrontonasal Dysplasia Information / Diagnosis / Treatment / Prevention External links (marked with an arrow ) open in a new window. This site is a web directory and does not offer medical advice. We cannot take responsibility for information found on listed sites. This Page Related Topics Health News Web Directory: Related Topics: Rare Disorders Health News: Search millions of published articles for news on Craniofrontonasal Dysplasia Modern Medicine Aging The Ardell Wellness Report HealthFacts Medical Post Medical Update Men's Health and the National Women's Health Report Note: Subscription required to access the full text of articles. Web Directory: National Library of Medicine: CNFS Offers synonyms of craniofrontonasal syndrome, a summary and a list of features. NORD: Craniofrontonasal Dysplasia Offers a general discussion and resources. OMIM: National Center for Biotechnology Information A clinical synopsis of Craniofrontonasal Dysplasia. Notes: Healthcyclopedia presents health information in the form of websites and articles that encompass conventional medicine and alternative treatments Under no circumstances can it recommend or endorse a specific drug or therapy or treatment.

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

9. Syndrome DB - Table Of Contents cerebellotrigeminal and focal dermal dysplasia. cerebellotrigeminaldermal dysplasia craniofrontonasal dysostosis. craniofrontonasal dysplasia (CFND) craniofrontonasal syndrome (CNFS http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_c.html

10. Search: - Info.co.uk Results for craniofrontonasal dysplasia from Info.co.uk metasearch. Find better search results from the Web, Yellow Pages and White Pages quickly and easily! Disorders CraniofrontonasaldysplasiaCraniofrontona saldysplasia SEARCH ENGINE WEBSEARCH Craniofrontonasaldysplasia http://dpxml.infospace.com/infocom.uk/results?otmpl=dog/webresults.htm&qkw=C

11. Result Of Search DEFECTS; MICROPHTHALMIA X;p;ter22 X-LINKED ICHTHYOSIS X;p;ter-22?craniofrontonasal dysplasia No cytogenetic aberrations matched http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-id-look2.pl?X p 22-11

12. ORPHANET - Rare Diseases - Orphan Drugs D I S E A S E craniofrontonasal dysplasia. ICD Q75.8 http://orphanet.infobiogen.fr/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1520

13. Disease Directory : Genetic Disorders : Craniofrontonasal Dysplasia Diseases Genetic Disorders craniofrontonasal dysplasia. »»CraniofrontonasalDysplasia Movie Reviews«« craniofrontonasal dysplasia Movie Reviews. http://www.diseasedirectory.net/Genetic_Disorders/Craniofrontonasal_Dysplasia/de

Wednesday, June 02, 2004 Genetic Disorders Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Craniofrontonasal Dysplasia »»Craniofrontonasal Dysplasia Movie Reviews«« - Craniofrontonasal Dysplasia Movie Reviews. Related Subjects: Genetic_Disorders. Family movie reviews for "Craniofrontonasal Dysplasia A family with craniofrontonasal dysplasia, and fragile site 12q13 ... - A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently. Kumar D, Clark JW, Blank CE, Patton MA. Conditions and Diseases: Genetic Disorders: Craniofrontonasal ... Craniofrontonasal Dysplasia - Craniofrontonasal (CFND) Dysplasia. NORD - Craniofrontonasal Dysplasia - http://www.stepstn.com Offers alternate names, a general discussion and resources. Craniofrontonasal Dysplasia - Craniofrontonasal Dysplasia Directory: Guide to Craniofrontonasal Dysplasia sites on the internet. Craniofrontonasal Dysplasia. Craniofrontonasal Dysplasia : Meddie Health Search - (Rating: 0.00 Votes: 0) Rate It. OMIM: National Center for Biotechnology Information A clinical synopsis of Craniofrontonasal Dysplasia. Craniofrontonasal Dysplasia @ www.Sweden.org

14. Disease Directory : Craniofrontonasal Dysplasia. Diseases Genetic Disorders craniofrontonasal dysplasia Craniofrontonasaldysplasia. Directory Listing. Title craniofrontonasal dysplasia. http://www.diseasedirectory.net/detailed/25019.aspx

Wednesday, June 02, 2004 Genetic Disorders Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome ... Craniofrontonasal Dysplasia : Craniofrontonasal dysplasia. Directory Listing Title: Craniofrontonasal dysplasia. Description: Craniofrontonasal dysplasia. Kapusta L, Brunner HG, Hamel BC. We report on nine patients with craniofrontonasal dysplasia (CFND). Date Added: 2/16/2004 2:22:40 PM URL:

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

document.write(''); var hwPrint=1; var hwDocHWID="nord1049"; var hwDocTitle="Craniofrontonasal Dysplasia"; var hwRank="1"; var hwSectionHWID="nord1049"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Craniofrontonasal Dysplasia Important It is possible that the main title of the report 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 Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Aarskog syndrome Frontofacionasal dysplasia Greig cephalopolysyndactyly syndrome Frontonasal dysplasia Orocraniodigital syndrome 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.

16. Orocraniodigital Syndrome craniofrontonasal dysplasia is a rare inherited disorder characterized by widelyspacedeyes (ocular hypertelorism), a missing or grooved tip of the nose, a http://www.bchealthguide.org/kbase/nord/nord1048.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord1048"; var hwDocTitle="Orocraniodigital Syndrome"; var hwRank="1"; var hwSectionHWID="nord1048"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Orocraniodigital Syndrome Important It is possible that the main title of the report 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 Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Craniofrontonasal Dysplasia Oral-Facial-Digital Syndrome (All Types) Frontofacionasal Dysplasia Frontonasal Dysplasia (Median Cleft Face Syndrome) 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.

17. Health Library - craniofrontonasal dysplasia. craniofrontonasal dysplasia follows Xlinked inheritancein most families, but females are more severely affected than males. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

18. Genetic Disorders, Craniofrontonasal Dysplasia More craniofrontonasal dysplasia Categories » Submit Your Site to the CraniofrontonasalDysplasia category. Sponsored craniofrontonasal dysplasia Sites. http://www.iseekhealth.com/craniofrontonasal_dysplasia-1554.php

Home About Us Contact Submit Your Site Search : Home Health Conditions and Diseases Genetic Disorders ... Craniofrontonasal Dysplasia More Craniofrontonasal Dysplasia Categories: Submit Your Site to the Craniofrontonasal Dysplasia category Sponsored Craniofrontonasal Dysplasia Sites Cystic Fibrosis Book Store At WellnessBooks.com Comprehensive source to books on Cystic Fibrosis. Includes community boards and chat, book reviews and online ordering. Buy Genetic Disorders Products We link to merchants which offer Genetic Disorders products for sale. Online Doctors - Ask Us Now! Kasamba's variety of health experts- including Doctors, Specialists, Herbalists, Nurses and more- offer real help for affordable consultation fees- live via chat or e-mail! Buy Genetics Books At Amazon.com and Save! Would you like to save on Genetics Books at Amazon and other stores? Compare prices at BookSellersNow.com! Our site continually proves that online shopping can be fun! National Library of Medicine: CNFS - Offers synonyms of craniofrontonasal syndrome, a summary and a list of features.

19. Genetic Disorders, Craniofrontonasal Dysplasia Category Home Health Conditions and Diseases Genetic Disorders craniofrontonasal dysplasia. * Site Title · The name of the site. http://www.iseekhealth.com/directory/index.php?method=show_link_exchange&directo

20. Craniofrontonasal Dysplasia craniofrontonasal dysplasia Important It is possible that the main title ofthe report craniofrontonasal dysplasia is not the name you expected. http://my.webmd.com/hw/health_guide_atoz/nord1049.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Quizzes, Calculators Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... 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.

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