Clinical Nuclear Medicine - UserLogin An 18year-old girl with cleidocranial dysplasia (CLCD) was admitted to our clinicfor cleidocranial dysplasia; bone scintigraphy; clavicular defect http://www.nuclearmed.com/pt/re/cnm/fulltext.00003072-200401000-00018.htm
Extractions: ExPASy Home page Site Map Search ExPASy Contact us Swiss-Prot Search Swiss-Prot/TrEMBL Swiss-Prot/TrEMBL (full text) PROSITE SWISS-2DPAGE ENZYME NEWT Taxonomy HAMAP families ExPASy web site for The ExPASy Server requires Javascript to be fully functional. You may not see all the information available for this page (More information) Entry info Name and origin References Comments ... Tools Note: most headings are clickable, even if they don't appear as links. They link to the user manual or other documents Entry information Entry name Primary accession number Secondary accession numbers Entered in Swiss-Prot in Release 41, February 2003 Sequence was last modified in Release 41, February 2003 Annotations were last modified in Release 48, September 2005 Name and origin of the protein Protein name Runt-related transcription factor 2 Synonyms Core-binding factor, alpha 1 subunit
Entrez PubMed cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia associatedwith clavicle hypoplasia and dental abnormalities. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Entrez PubMed Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential forosteoblast differentiation and bone development. Otto F, Thornell AP, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9
CCDD: Family: Education: Descriptions Of Disorders cleidocranial dysplasia (Cleidocranial Dysostosis) cleidocranial dysplasia isa genetic condition that features problems with the development of bones and http://www.hopkinsmedicine.org/craniofacial/Education/Disorders.cfm?Source=Famil
OMIM Entry 600211 .0002 cleidocranial dysplasia. RUNX2, TRP283TER. A sporadic case of cleidocranialdysplasia (119600) was found to be caused by heterozygosity for a Gto-A http://www.hgmp.mrc.ac.uk/cgi-bin/wrapomim?600211
Orthoguide.com Cleidocranial Dysplasia Search AltaVista for cleidocranial dysplasia Global Search Add Url - FreeMedline - Contact Us - Search. Enter Keywords to Search and Your Choice of http://www.orthoguide.com/ortho/Cleidocranial_Dysplasia.php3
Opera Directory MedicineNet.com cleidocranial dysplasia. Basic information. National Library ofMedicine cleidocranial dysplasia (CCD, CLCD) http://portal.opera.com/web/?cat=523622
Expression And Functions Of TCF-4 In Cleidocranial Dysplasia cleidocranial dysplasia (CCD) is an autosomal dominant disease resulting inclavicle hypoplasia, patent fontanel, lack of primary teeth resorption, http://iadr.confex.com/iadr/2004Hawaii/techprogram/abstract_47852.htm
Molecular Mechanisms Of Cleidocranial Dysplasia cleidocranial dysplasia (CCD), characterized by abnormal bone, tooth and periodontaltissue formation and supernumerary and impacted teeth, http://iadr.confex.com/iadr/2004Hawaii/techprogram/abstract_47822.htm
Extractions: This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Silverman, F. N. Articles by Reiley, M. A. FN Silverman and MA Reiley Eight patients are presented who have a generalized bone dysplasia that resembles severe cleidocranial dysplasia but lacks the cranial and clavicular features of that well-defined condition. Vertebral-body ossification is markedly defective, and ossification centers of the tubular bones are grossly enlarged. These patients also differ from those with variant forms of cleidocranial dysplasia described in the literature. It is
Bioline International Official Site (site Up-dated Regularly) A diagnosis of cleidocranial dysplasia was made. Discussion. cleidocranial dysplasiais an autosomal dominant condition with generalised dysplasia of bone http://www.bioline.org.br/request?jp01058
Pregnancy & Parenting: For Today's Mom - IVillage A Case of cleidocranial dysplasia Confirmed by 3D CT of the cleidocranial dysplasia (CCD) is an autosomal dominant disorder Facial anddental anomalies in cleidocranial dysplasia a study of 17 cases. http://www.parentsplace.com/expert/dentist/general/qa/0,3459,6766,00.html
Extractions: var iv_cimsUid = ""; var iv_cimsCid = "12"; // Tacoda category stamp var dartCatStamp = "parenting"; Tacoda_AMS_DDC_addPair("dartCatStamp", dartCatStamp); @import "/shared/css/global/0,,,00.css"; @import "/shared/css/touts/0,,,00.css"; @import "/shared/css/layout/0,,flyout,00.css"; @import "/shared/css/content/0,,channelhome,00.css"; @import "/shared/css/channel/0,,12,00.css"; Skip to Main Content iVillage web Pregnancy Baby Toddler/ Preschooler Grade-Schooler Tween Teen Being a Mom Stuff We Love Family Time Activities Baby Names ... Peg Plumbo, CNM, Nurse-Midwife
UW Radiology Main Online Teaching File: Case 45 Answers dysplasia indicates an abnormality in the development of bone, and cleido (clavicle)and cranial (head) tell us where major abnormalities occur. http://www.rad.washington.edu/maintf/cases/unk45/answers.html
Extractions: UW Radiology Main Online Teaching File UW Radiology Home Unknown Cases in Random Order Musculoskeletal Cases Only Breast Cases Only ... Search this site UW Radiology Main Online Teaching File: Case 45 Answers Cleidocranial dysplasia. PA radiograph of the chest This is an autosomal dominant disorder whose very name tells us a lot about it. Dysplasia indicates an abnormality in the development of bone, and cleido- (clavicle) and cranial (head) tell us where major abnormalities occur. This disorder occurs in both membranous and enchondral bone, and has a striking propensity for affecting midline structures. If you painted a big, broad stripe down the midline with a paintbrush from skull to groin, you'd paint over a lot of structures involved with this syndrome. Prominent features include a large head with delayed suture closure, Wormian bones, hypertelorism, a small face, dental dysplasia, hypoplasia or aplasia of the clavicles, a narrow pelvis, and several varieties of spinal abnormalities. Just about every other bone in the body may be involved as well, including the ossicles of the ear. Despite the midline tendency, the appendicular skeleton is also frequently involved. AP radiographs of the skull and pelvis.
