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Craniofrontonasal Dysplasia:     more detail

lists with details

21. Opera Directory
    NORD craniofrontonasal dysplasia. Offers a general discussion and resources . A clinical synopsis of craniofrontonasal dysplasia.  
    http://portal.opera.com/directory/?cat=525006

22. Entrez PubMed
    craniofrontonasal dysplasia more severe expression in the mother than in herson We report a famil  
    http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8

23. Entrez PubMed
    craniofrontonasal dysplasia (CFND) was diagnosed in a male child who had bilateralcoronal craniosyn  
    http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8

24. 304110 CRANIOFRONTONASAL SYNDROME; CFNS
    craniofrontonasal dysplasia (CFND), or craniofrontonasal syndrome (CFNS), Sax, CM; Flannery, DB craniofrontonasal dysplasia clinical and genetic  
    http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:304110] -e

25. %145420 HYPERTELORISM, TEEBI TYPE
    with some other features suggesting craniofrontonasal dysplasia (CFND; AS New autosomal dominant syndrome resembling craniofrontonasal dysplasia.  
    http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:145420] -e

26. Plastic And Maxillofacial Surgery : Research
    Neuropsychological profiles of children with craniofrontonasal dysplasia.craniofrontonasal dysplasia is a rare, familial craniofacial syndrome that results  
    http://www.rch.org.au/plastic/research.cfm
    
    Extractions: Print version Peter G. Farlie Some of our current research projects include: Genetic Health Services Victoria: Prof Agnes Bankier, Dr Sue White The repair of congenital or acquired defects in the secondary palate and cranial bones remains a significant clinical challenge. The availability of reliable, widely applicable biomaterials to augment the range of surgical approaches utilized in the repair of palate and calvarial defects would greatly enhance management of these conditions. In collaboration with the Department of Chemical and Biomolecular Engineering, University of Melbourne, we are developing a research program with a focus on the application of existing biomaterials and the development of novel modifications. These materials will facilitate enhanced biointegration and the use of patient derived chrondrogenic and osteogenic precursors for tissue engineering. Craniofacial development: characterising the molecular regulators

27. Clinical Dysmorphology - UserLogin
    New autosomal dominant syndrome resembling craniofrontonasal dysplasia. Am J MedGenet 28581591. Medline Link CrossRef Context Link  
    http://www.clindysmorphol.com/pt/re/mcd/fulltext.00019605-200307000-00008.htm

28. Clinical Dysmorphology - UserLogin
    Craniofrontonasal syndrome or dysplasia (CFNS, OMIM 304110) is characterized Further evidence from two families that craniofrontonasal dysplasia maps to  
    http://www.clindysmorphol.com/pt/re/mcd/fulltext.00019605-200204000-00019.htm

29. Health Library -
    Journal of Craniofacial Surgery Fulltext Volume 12(3) May 2001 Cohen has reported the condition of craniofrontonasal dysplasia, whereby midline Cohen Jr. MM craniofrontonasal dysplasia. Birth Defects 1979; 1585-89  
    http://12.42.224.150/library/healthguide/en-us/illnessconditions/topic.asp?hwid=

30. Journal Of Craniofacial Surgery - UserLogin
    (Below) craniofrontonasal dysplasia (Xp22). Note orbital hypertelorism, bifid nose, craniofrontonasal dysplasia. Br J Plast Surg 1997; 50153161  
    http://www.jcraniofacialsurgery.com/pt/re/jcransurg/fulltext.00001665-200201000-

31. Birth Disorder Information Directory - CO-CZ
    craniofrontonasal dysplasia/Syndrome. craniofrontonasal dysplasia CRANIOFRONTONASALSYNDROME; CFNS. Craniofrontonasal Syndrome. Teebi Type  
    http://www.bdid.com/defectco.htm
    
    Extractions: HOME COACH Syndrome Coarctation of (the) Aorta (CoA) Coats' Disease (Congenital Retinal Telangiectasia, Exudative Retinitis, Leber Miliary Aneurysm) Cobb Syndrome Cocaine Antenatal Infection Cochin Jewish Disorder (Haim Munk Syndrome, Keratosis Palmoplantaris Periodontopathia) Cockayne Syndrome COD-MD Syndrome CODAS Syndrome (Cerebrooculodentoauriculoskeletal Syndrome) Coffin Syndrome (Arthritis Short Stature Deafness) Coffin-Lowry Syndrome Coffin Siris Syndrome (Fifth Digit Syndrome) COFS Syndrome Cohen Hayden Syndrome (Proteus-Like Syndrome with Mental Retardation and Eye Defects) Cohen Lockood Wyborney Syndrome (Blepharophimosis Ptosis Syndactyly Mental Retardation) Cohen Syndrome Colavita Kozlowski Syndrome (Short Limb Dwarf, Lethal Colavita Kozlowski Type)

32. Health Library -
    Indian Pediatrics Editorialcraniofrontonasal dysplasia is another entity which is distinguished from Clinically these patients of craniofrontonasal dysplasia are observed to have  
    http://12.31.13.113/library/healthguide/en-us/illnessconditions/topic.asp?hwid=n

33. GeneCard For CFNS
    craniofrontonasal syndrome (craniofrontonasal dysplasia) Symbol approved by theHUGO Gene Nomenclature Committee (HGNC) database  
    http://www.nbn.ac.za/genecards/cgi-bin/carddisp?CFNS

34. Plastic And Reconstructive Surgery - UserLogin
    Cohen Syndrome, Craniofrontal Dysplasia, Craniofrontonasal Dysostosis, Craniofrontonasal craniofrontonasal dysplasia was the second most common cause of  
    http://www.plasreconsurg.com/pt/re/prs/fulltext.00006534-199702000-00004.htm

35. Plastic And Reconstructive Surgery - UserLogin
    The most common diagnosis was frontonasal dysplasia (64.3 percent), followed bycraniofrontonasal dysplasia (14.3 percent), Crouzon syndrome (14.3 percent),  
    http://www.plasreconsurg.com/pt/re/prs/fulltext.00006534-200505000-00010.htm

36. AOJ 52:58 "Ocular Aspects Of Craniofacial Disorders"
    craniofrontonasal dysplasia is an Xlinked dominant condition, in which femalesonly are affected. There is often marked Hypertelorism, craniosynostoses and  
    http://www.aoj.org/abstracts/52/52_58.html
    
    Extractions: Am Orthopt J 52:58 (2002). John Pratt-Johnson Lecture Ocular Aspects of Craniofacial Disorders Ken K. Nischal, F.R.C., Ophth. Craniofacial disorders may comprise various entities such as clefting anomalies, tumors, e.g., fibrous dysplasia, orbito-facio-cranial trauma, and the craniosynostoses. Each may have significant ocular involvement but the focus of my discussion is the craniosynostoses. Craniosynostosis is the premature closure of one or more cranial sutures and this may be associated with systemic features or an isolated finding. When a suture closes prematurely growth of the skull continues parallel to the suture but is arrested or retarded perpendicular to it. This results in an irregular shape of the skull. Previously patients with suture synostosis were described as having a particular shaped head such as plagiocephaly, brachycephaly, or scaphocephaly to name a few. These are now better described in terms of the sutures involved, e.g., plagiocephaly is better described as unicoronal synostosis, brachycephaly as bicoronal synostosis, and scaphocephaly as sagittal synostosis. © 2002 The Board of Regents of the University of Wisconsin System

37. Centre For Genetics Education:: Disorder Information And Support
    craniofrontonasal dysplasia Craniosynostosis Syndromes Creutzfeldt Jakob DiseaseCri Du Chat Syndrome Crohn Disease Crouzon Syndrome Currarino Syndrome  
    http://www.genetics.com.au/conditions/main.htm

38. A Novel Phenotypic Pattern In X-linked Inheritance: Craniofrontonasal Syndrome M
    4 Cohen , MM , Jr ( 1979 ) craniofrontonasal dysplasia. 6 Grutzner , E.and Gorlin, RJ ( 1988 ) craniofrontonasal dysplasia phenotypic expression in  
    http://hmg.oxfordjournals.org/cgi/content/full/6/11/1937
    
    Extractions: This Article Abstract FREE Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Cited by other online articles Search for citing articles in:

39. Karger Publishers
    Grutzner E, Gorlin RJ craniofrontonasal dysplasia phenotypic expression McPherson E, Estop A, PaulusThomas J craniofrontonasal dysplasia in a girl  
    http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=

40. Resources For Genetic Counselors - Frontonasal Dysplasia - Median Cleft Face Syn
    C. craniofrontonasal dysplasia VII. Resources A. Children s CraniofacialAssociation (CCA) Phone (800) 5353643 Email contactcca@ccakids.com  
    http://www.genesoc.com/counseling2/article77.html

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