Literature DB >> 1058439

The disturbances in odontogenesis in epidermolysis bullosa hereditaria letalis.

D G Gardner, C D Hudson.   

Abstract

The disturbances in odontogenesis in a case of epidermolysis bullosa hereditaria letalis are described, with particular emphasis on the morphologic alterations in the ameloblasts and on the nature of vesicles in the enamel organ. These latter structures are compared to those found in the skin.

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Year:  1975        PMID： 1058439     DOI： 10.1016/0030-4220(75)90246-7

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol        ISSN： 0030-4220


  3 in total

1.  Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition.

Authors:  J A McGrath; B Gatalica; K Li; M G Dunnill; J R McMillan; A M Christiano; R A Eady; J Uitto
Journal:  Am J Pathol       Date:  1996-06       Impact factor: 4.307

2.  Targeted disruption of the LAMA3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells.

Authors:  M C Ryan; K Lee; Y Miyashita; W G Carter
Journal:  J Cell Biol       Date:  1999-06-14       Impact factor: 10.539

3.  Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa.

Authors:  Susanne Krämer; James Lucas; Francisca Gamboa; Miguel Peñarrocha Diago; David Peñarrocha Oltra; Marcelo Guzmán-Letelier; Sanchit Paul; Gustavo Molina; Lorena Sepúlveda; Ignacio Araya; Rubén Soto; Carolina Arriagada; Anne W Lucky; Jemima E Mellerio; Roger Cornwall; Fatimah Alsayer; Reinhard Schilke; Mark Adam Antal; Fernanda Castrillón; Camila Paredes; Maria Concepción Serrano; Victoria Clark
Journal:  Spec Care Dentist       Date:  2020-11
  3 in total

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