Extractions: Related links of interest: 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. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The combose.com directory is based on the Open Directory and has been modified and enhanced using our own technology. About ComboSE Download Combose Toolbar
Craniofrontonasal Dysplasia craniofrontonasal dysplasia. Abnormalities of the head and face, handsand feet and skeletal bones typify this rare, inherited disorder. http://www.forwardface.org/misc_text/conditions/craniofront.htm
Extractions: 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.
Genetic Disorders: Craniofrontonasal Dysplasia Genetic Disorders craniofrontonasal dysplasia. features. NORD CraniofrontonasalDysplasia. Offers a general discussion and resources. http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/Cr
Craniofrontonasal Dysplasia The New Health Directory, Directory, Home Health Conditions and DiseasesGenetic Disorders craniofrontonasal dysplasia (3) See Also http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/Cr
:: Ez2Find :: Craniofrontonasal Dysplasia Guide craniofrontonasal dysplasia, Global Metasearch Any Language Guides,craniofrontonasal dysplasia. ez2Find Home Directory Health http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Craniofrontonasal Dysplasia Web Sites National Library of Medicine: CNFS [Site Info] [Translate] [Open New Window] NORD: Craniofrontonasal Dysplasia [Site Info] [Translate] [Open New Window] Offers a general discussion and resources. URL: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Craniofrontonasal%20Dysplasia
Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Rare Disorders Web Sites National Organization for Rare Disorders, Inc. [Site Info] [Translate] [Open New Window] Information about NORD, its programs, special events and the variety of services offered. Includes a rare disease, organization and orphan drug database. Diseases are listed alphabetically for easy searching. URL: http://www.rarediseases.org/
Craniofrontonasal Dysplasia : Meddie Health Search (Rating 0.00 Votes 0) Rate It. OMIM National Center for BiotechnologyInformation A clinical synopsis of craniofrontonasal dysplasia. http://www.meddie.com/Conditions_and_Diseases/Genetic_Disorders/Craniofrontonasa
Entrez PubMed craniofrontonasal dysplasia. Kapusta L, Brunner HG, Hamel BC. We reporton nine patients with craniofrontonasal dysplasia (CFND). http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra
Entrez PubMed A family with craniofrontonasal dysplasia, and fragile site 12q13 segregatingindependently. Kumar D, Clark JW, Blank CE, Patton MA. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra
Health Library - craniofrontonasal dysplasia. craniofrontonasal dysplasia follows Xlinked inheritancein most families, but females are more severely affected than males. http://healthlink.uhseast.com/Library/HealthGuide/IllnessConditions/topic.asp?hw
Health Library - craniofrontonasal dysplasia. Important It is possible that the main title ofthe report craniofrontonasal dysplasia is not the name you expected. http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=
Health Library - craniofrontonasal dysplasia. Important It is possible that the main title ofthe report craniofrontonasal dysplasia is not the name you expected. http://12.31.13.29/library/healthguide/IllnessConditions/topic.asp?hwid=nord1049
