Literature DB >> 7084543

Epidermolysis bullosa herpetiformis Dowling-Meara. Report of a case and pathomorphogenesis.

I Anton-Lamprecht, U W Schnyder.   

Abstract

Report of a 2-year-old girl of Turkish origin with congenital generalized blister formation in herpetiform arrangement. Direct immunofluorescence ruled out juvenile dermatitis herpetiformis Duhring. Ultrastructural investigation of a fresh blister and clinically intact preblistering skin revealed intraepidermal blister formation via cytolysis of basal cells preceded by clumping of tonofilaments and partial attachment to the hemidesmosomes at the dermo-epidermal junction. This type of blister formation is significantly different from all other epidermolysis bullosa types and is a characteristic feature of all further cases studied so far by electron microscopy (n = 20) which correspond to the original cases of Dowling and Meara. Clinical features characteristic of this epidermolysis type are outlined and classification of epidermolysis bullosa herpetiformis Dowling-Meara into the non-scarring epidermolyses with dominant inheritance is discussed.

Entities:  

Mesh:

Year:  1982        PMID: 7084543

Source DB:  PubMed          Journal:  Dermatologica        ISSN: 0011-9075


  23 in total

1.  Epidermolysis bullosa simplex-type mutations alter the dynamics of the keratin cytoskeleton and reveal a contribution of actin to the transport of keratin subunits.

Authors:  Nicola Susann Werner; Reinhard Windoffer; Pavel Strnad; Christine Grund; Rudolf Eberhard Leube; Thomas Michael Magin
Journal:  Mol Biol Cell       Date:  2003-12-10       Impact factor: 4.138

Review 2.  Epidermolysis bullosa: hereditary skin fragility diseases as paradigms in cell biology.

Authors:  R A Eady; M G Dunnill
Journal:  Arch Dermatol Res       Date:  1994       Impact factor: 3.017

3.  Vesiculo-bullous disorders in childhood.

Authors:  R M McKay
Journal:  Can Fam Physician       Date:  1987-11       Impact factor: 3.275

4.  Very late antigen (VLA) expression in various forms of epidermolysis bullosa simplex.

Authors:  V Nazzaro; E Berti; R Cavalli; A Brusasco; R Caputo
Journal:  Arch Dermatol Res       Date:  1991       Impact factor: 3.017

Review 5.  Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton.

Authors:  E Fuchs
Journal:  Mol Biol Cell       Date:  1997-02       Impact factor: 4.138

6.  Eosinophil infiltration in three patients with generalized atrophic benign epidermolysis bullosa from a Japanese family: molecular genetic and immunohistochemical studies.

Authors:  Masayo Nomura; Yoh-Ichiro Hamasaki; Ichiro Katayama; Kuniko Abe; Norio Niikawa; Koh-Ichiro Yoshiura
Journal:  J Hum Genet       Date:  2005-09-20       Impact factor: 3.172

7.  Epidermolysis bullosa herpetiformis (Dowling-Meara type) exhibits ultrastructural derangement of tonofilaments and desmosomes.

Authors:  M Furumura; S Imayama; Y Hori
Journal:  Arch Dermatol Res       Date:  1994       Impact factor: 3.017

8.  Prenatal diagnosis of genetic disorders of the skin by means of electron microscopy.

Authors:  I Anton-Lamprecht
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 9.  The molecular basis for inherited bullous diseases.

Authors:  B P Korge; T Krieg
Journal:  J Mol Med (Berl)       Date:  1996-02       Impact factor: 4.599

10.  Linkage of epidermolysis bullosa simplex to keratin gene loci.

Authors:  K E McKenna; A E Hughes; E A Bingham; N C Nevin
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

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