[Juvenile periodontopathies as a manifestation of an ectodermal abnormality].
Identifieur interne : 003509 ( Ncbi/Checkpoint ); précédent : 003508; suivant : 003510[Juvenile periodontopathies as a manifestation of an ectodermal abnormality].
Auteurs : B. RinkSource :
- Kinderarztliche Praxis [ 0023-1495 ] ; 1990.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
Abstract
By means of three cases of progressive infantile periodontal diseases the author points at simultaneous alteration in the keratinization of the skin in the sense of keratosis palmaris et plantaris (Papillon-Lefèvre-Disease). This complex of anomalies is supposed to be a hereditary acro-ectodermal systemic inferiority, primarily consisting in an epithelial disturbance. But it is also necessary to regard the infantile progressive periodontal insufficiency as an obligatory or facultative attendant symptom of general diseases. The therapy is only symptomatic, complete return to health is not realizable.
PubMed: 2141375
Affiliations:
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pubmed:2141375Le document en format XML
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<affiliation><nlm:affiliation>Klinik für Kiefer- und Gesichtschirurgie, Bereichs Medizin (Charité) der Humboldt-Universität zu Berlin.</nlm:affiliation>
<wicri:noCountry code="subField">Bereichs Medizin (Charité) der Humboldt-Universität zu Berlin</wicri:noCountry>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aggressive Periodontitis (genetics)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Genes, Recessive</term>
<term>Gingival Hyperplasia (genetics)</term>
<term>Humans</term>
<term>Keratoderma, Palmoplantar (genetics)</term>
<term>Male</term>
<term>Mouth, Edentulous (genetics)</term>
<term>Periodontal Diseases (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Bouche édentée (génétique)</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Gènes récessifs</term>
<term>Humains</term>
<term>Hyperplasie gingivale (génétique)</term>
<term>Kératose palmoplantaire (génétique)</term>
<term>Maladies parodontales (génétique)</term>
<term>Mâle</term>
<term>Parodontite agressive (génétique)</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Aggressive Periodontitis</term>
<term>Gingival Hyperplasia</term>
<term>Keratoderma, Palmoplantar</term>
<term>Mouth, Edentulous</term>
<term>Periodontal Diseases</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Bouche édentée</term>
<term>Hyperplasie gingivale</term>
<term>Kératose palmoplantaire</term>
<term>Maladies parodontales</term>
<term>Parodontite agressive</term>
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<term>Female</term>
<term>Genes, Recessive</term>
<term>Humans</term>
<term>Male</term>
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<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Gènes récessifs</term>
<term>Humains</term>
<term>Mâle</term>
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<front><div type="abstract" xml:lang="en">By means of three cases of progressive infantile periodontal diseases the author points at simultaneous alteration in the keratinization of the skin in the sense of keratosis palmaris et plantaris (Papillon-Lefèvre-Disease). This complex of anomalies is supposed to be a hereditary acro-ectodermal systemic inferiority, primarily consisting in an epithelial disturbance. But it is also necessary to regard the infantile progressive periodontal insufficiency as an obligatory or facultative attendant symptom of general diseases. The therapy is only symptomatic, complete return to health is not realizable.</div>
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