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
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
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
Extractions: 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).
Extractions: 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.
Extractions: 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.
Redirect A clinical synopsis of craniofrontonasal dysplasia. http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?304110
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
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
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
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
Extractions: 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
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
Extractions: 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. Information on the following diseases can be found in the Related Disorders section of this report: 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.
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
Extractions: 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. Information on the following diseases can be found in the Related Disorders section of this report: 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.
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
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
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
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
Extractions: 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.
