Literature DB >> 19543698

[Skin and teeth].

J Heinlin1, N Heinlin, J Steinbauer, M Landthaler, S Karrer.   

Abstract

Skin and teeth not only share several characteristics in their development but also have a similar ontogenetic origin from the ectoderm. Thus, numerous congenital diseases, such as genetic, infectious, inflammatory, and immune disorders affect both skin and teeth. Particularly skin diseases are often identified by the synopsis of systemic symptoms. The understanding and appreciation of dental abnormalities guides dermatologists in the diagnosis and identification of syndromes as well as in finding an optimal therapy.

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Year:  2009        PMID: 19543698     DOI: 10.1007/s00105-009-1789-y

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  83 in total

1.  A new family with Papillon-Lefèvre syndrome: effectiveness of etretinate treatment.

Authors:  M Siragusa; C Romano; N Batticane; D Batolo; C Schepis
Journal:  Cutis       Date:  2000-03

Review 2.  Successful periodontal maintenance of a case with Papillon-Lefèvre syndrome: 12-year follow-up and review of the literature.

Authors:  C B Wiebe; L Häkkinen; E E Putnins; P Walsh; H S Larjava
Journal:  J Periodontol       Date:  2001-06       Impact factor: 6.993

Review 3.  Dental manifestations of dermatologic conditions.

Authors:  Anatoli Freiman; Daniel Borsuk; Benjamin Barankin; Geoffrey H Sperber; Bernice Krafchik
Journal:  J Am Acad Dermatol       Date:  2008-11-22       Impact factor: 11.527

Review 4.  Langerhans cell histiocytosis: literature review and descriptive analysis of oral manifestations.

Authors:  Cristina Madrigal-Martínez-Pereda; Vanesa Guerrero-Rodríguez; Blanca Guisado-Moya; Cristina Meniz-García
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2009-05-01

5.  Single maxillary central incisor and coloboma in hypomelanosis of Ito.

Authors:  D W Bartholomew; E W Jabs; L S Levin; R Ribovich
Journal:  Clin Genet       Date:  1987-06       Impact factor: 4.438

Review 6.  Recent progress in the genetics of incontinentia pigmenti (Bloch-Sulzberger syndrome).

Authors:  B S Shastry
Journal:  J Hum Genet       Date:  2000       Impact factor: 3.172

7.  Hamartomatous dental cusps in hypomelanosis of Ito.

Authors:  R Happle; F Vakilzadeh
Journal:  Clin Genet       Date:  1982-01       Impact factor: 4.438

8.  Oral conditions in Sjögren-Larsson syndrome.

Authors:  H Forsberg; S Jagell; C O Reuterving
Journal:  Swed Dent J       Date:  1983

9.  A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.

Authors:  M Naeem; M Wajid; K Lee; S M Leal; W Ahmad
Journal:  J Med Genet       Date:  2006-03       Impact factor: 6.318

10.  Polyposis coli, craniofacial exostosis and astrocytoma: the concomitant occurrence of the Gardner's and Turcot syndromes.

Authors:  R W Koot; T J Hulsebos; J J van Overbeeke
Journal:  Surg Neurol       Date:  1996-03
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