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
Extractions: 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. 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.
Redirect A clinical synopsis of craniofrontonasal dysplasia. http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?304110
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
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
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.
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
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
Extractions: 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. 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. Children's Craniofacial Association
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
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
Extractions: 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. 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. Children's Craniofacial Association
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
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
Extractions: 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. 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. Children's Craniofacial Association
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
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
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.
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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
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
