Clinical aspects of dental anomalies.
Identifieur interne : 000754 ( Main/Exploration ); précédent : 000753; suivant : 000755Clinical aspects of dental anomalies.
Auteurs : C J WitkopSource :
- International dental journal [ 0020-6539 ] ; 1976.
Descripteurs français
- KwdFr :
- Aberrations des chromosomes (complications), Cavité pulpaire de la dent (anatomopathologie), Cavité pulpaire de la dent (malformations), Dentinogenèse imparfaite (complications), Dysplasie de la dentine (complications), Dysplasies osseuses (complications), Humains (MeSH), Hypophosphatasie (complications), Hypophosphatémie familiale (complications), Maladies chromosomiques (MeSH), Malformations dentaires (anatomopathologie), Odontodysplasie (complications), Phosphore (sang), Populations d'origine continentale (MeSH), Pseudohypoparathyroïdie (complications), Rachitisme (complications), Syndrome (MeSH).
- MESH :
- anatomopathologie : Cavité pulpaire de la dent, Malformations dentaires.
- malformations : Aberrations des chromosomes, Cavité pulpaire de la dent, Dentinogenèse imparfaite, Dysplasie de la dentine, Dysplasies osseuses, Hypophosphatasie, Hypophosphatémie familiale, Odontodysplasie, Pseudohypoparathyroïdie, Rachitisme.
- sang : Phosphore.
- Humains, Maladies chromosomiques, Populations d'origine continentale, Syndrome.
English descriptors
- KwdEn :
- Bone Diseases, Developmental (complications), Chromosome Aberrations (complications), Chromosome Disorders (MeSH), Continental Population Groups (MeSH), Dental Pulp Cavity (abnormalities), Dental Pulp Cavity (pathology), Dentin Dysplasia (complications), Dentinogenesis Imperfecta (complications), Humans (MeSH), Hypophosphatasia (complications), Hypophosphatemia, Familial (complications), Odontodysplasia (complications), Phosphorus (blood), Pseudohypoparathyroidism (complications), Rickets (complications), Syndrome (MeSH), Tooth Abnormalities (pathology).
- MESH :
- chemical , blood : Phosphorus.
- abnormalities : Dental Pulp Cavity.
- complications : Bone Diseases, Developmental, Chromosome Aberrations, Dentin Dysplasia, Dentinogenesis Imperfecta, Hypophosphatasia, Hypophosphatemia, Familial, Odontodysplasia, Pseudohypoparathyroidism, Rickets.
- pathology : Dental Pulp Cavity, Tooth Abnormalities.
- Chromosome Disorders, Continental Population Groups, Humans, Syndrome.
Abstract
Many inherited disorders have oral manifestations which can be detected on dental radiographs as alterations in the morphology or chemical composition of the teeth. Thus the dentist may be the first to detect disorders of development and metabolism of importance to the general health of the patient and his family. In one group of conditions the pulp chamber is larger than normal. This may be associated with taurodontism in such conditions as polyploidy of the -X chromosome and trisomy-21 or Down's syndrome. Taurodontism also occurs in a variety of other syndromes including the tricho-dento-osseous syndrome described by Robinson, Miller and Worth (1966) and Mohr's syndrome. It may also be associated with scanty hair endoligodentia. In certain metabolic conditions the pulp chamber may be enlarged but the teeth are of relatively normal from (cynodont). Such cases include hypophosphatemic vitamin D-resistant and dependent rickets, pseudo-hypoparthyroidism otodental syndrome and hypophosphatasia. Small pulp chambers and associated anomalies of root morphology also occur in hereditary disorders either alone or as part of various syndromes such as dentino-osseous dysplasia and brackioskeletogenital syndrome. Dentinogenesis imperfecta may occur alone or as one manifestation of osteogenesis imperfecta. Other developmental defects including pulpal dysplasia, labodontia and dens invaginatus are also associated with small pulp chambers.
PubMed: 186412
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Thus the dentist may be the first to detect disorders of development and metabolism of importance to the general health of the patient and his family. In one group of conditions the pulp chamber is larger than normal. This may be associated with taurodontism in such conditions as polyploidy of the -X chromosome and trisomy-21 or Down's syndrome. Taurodontism also occurs in a variety of other syndromes including the tricho-dento-osseous syndrome described by Robinson, Miller and Worth (1966) and Mohr's syndrome. It may also be associated with scanty hair endoligodentia. In certain metabolic conditions the pulp chamber may be enlarged but the teeth are of relatively normal from (cynodont). Such cases include hypophosphatemic vitamin D-resistant and dependent rickets, pseudo-hypoparthyroidism otodental syndrome and hypophosphatasia. Small pulp chambers and associated anomalies of root morphology also occur in hereditary disorders either alone or as part of various syndromes such as dentino-osseous dysplasia and brackioskeletogenital syndrome. Dentinogenesis imperfecta may occur alone or as one manifestation of osteogenesis imperfecta. Other developmental defects including pulpal dysplasia, labodontia and dens invaginatus are also associated with small pulp chambers.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">186412</PMID><DateCompleted><Year>1977</Year><Month>01</Month><Day>28</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0020-6539</ISSN><JournalIssue CitedMedium="Print"><Volume>26</Volume><Issue>4</Issue><PubDate><Year>1976</Year><Month>Dec</Month></PubDate></JournalIssue><Title>International dental journal</Title><ISOAbbreviation>Int Dent J</ISOAbbreviation></Journal><ArticleTitle>Clinical aspects of dental anomalies.</ArticleTitle><Pagination><MedlinePgn>378-90</MedlinePgn></Pagination><Abstract><AbstractText>Many inherited disorders have oral manifestations which can be detected on dental radiographs as alterations in the morphology or chemical composition of the teeth. Thus the dentist may be the first to detect disorders of development and metabolism of importance to the general health of the patient and his family. In one group of conditions the pulp chamber is larger than normal. This may be associated with taurodontism in such conditions as polyploidy of the -X chromosome and trisomy-21 or Down's syndrome. Taurodontism also occurs in a variety of other syndromes including the tricho-dento-osseous syndrome described by Robinson, Miller and Worth (1966) and Mohr's syndrome. It may also be associated with scanty hair endoligodentia. In certain metabolic conditions the pulp chamber may be enlarged but the teeth are of relatively normal from (cynodont). Such cases include hypophosphatemic vitamin D-resistant and dependent rickets, pseudo-hypoparthyroidism otodental syndrome and hypophosphatasia. Small pulp chambers and associated anomalies of root morphology also occur in hereditary disorders either alone or as part of various syndromes such as dentino-osseous dysplasia and brackioskeletogenital syndrome. Dentinogenesis imperfecta may occur alone or as one manifestation of osteogenesis imperfecta. Other developmental defects including pulpal dysplasia, labodontia and dens invaginatus are also associated with small pulp chambers.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Witkop</LastName><ForeName>C J</ForeName><Initials>CJ</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013487">Research Support, U.S. Gov't, P.H.S.</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Int Dent J</MedlineTA><NlmUniqueID>0374714</NlmUniqueID><ISSNLinking>0020-6539</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>27YLU75U4W</RegistryNumber><NameOfSubstance UI="D010758">Phosphorus</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001848" MajorTopicYN="N">Bone Diseases, Developmental</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002869" MajorTopicYN="N">Chromosome Aberrations</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D025063" MajorTopicYN="N">Chromosome Disorders</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D044469" MajorTopicYN="N">Continental Population Groups</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003786" MajorTopicYN="N">Dental Pulp Cavity</DescriptorName><QualifierName UI="Q000002" MajorTopicYN="N">abnormalities</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003805" MajorTopicYN="N">Dentin Dysplasia</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003811" MajorTopicYN="N">Dentinogenesis Imperfecta</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007014" MajorTopicYN="N">Hypophosphatasia</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007015" MajorTopicYN="N">Hypophosphatemia, Familial</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018126" MajorTopicYN="N">Odontodysplasia</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010758" MajorTopicYN="N">Phosphorus</DescriptorName><QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011547" MajorTopicYN="N">Pseudohypoparathyroidism</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012279" MajorTopicYN="N">Rickets</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014071" MajorTopicYN="N">Tooth Abnormalities</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading></MeshHeadingList><NumberOfReferences>51</NumberOfReferences></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1976</Year><Month>12</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1976</Year><Month>12</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1976</Year><Month>12</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">186412</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Witkop, C J" sort="Witkop, C J" uniqKey="Witkop C" first="C J" last="Witkop">C J Witkop</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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