Literature DB >> 6208542

The ichthyoses--pathogenesis and prenatal diagnosis: a review of recent advances.

M L Williams.   

Abstract

Disturbances in the process of normal cornification leading to pathologic scaling provide the pathophysiologic basis for the ichthyoses. These disturbances may result from either abnormalities in protein metabolism (keratinization) (i.e., the "bricks") or in lipid metabolism (i.e., the "mortar") (Fig. 1). The evidence linking the various ichthyoses to defects in protein or lipid metabolism have been reviewed. It is likely that future advances will lead not only to a more complete understanding of the pathogenesis of these disorders, but also will shed significant light on the normal stratum corneum functions of barrier formation and desquamation, as well as lead the way to more rational and effective therapies. In recent years, prenatal diagnosis has been successfully performed in several of the ichthyoses. It is likely that improvements in our ability to prenatally diagnose those disorders will advance hand-in-hand with further progress in unraveling their underlying causes.

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Year:  1983        PMID: 6208542     DOI: 10.1111/j.1525-1470.1983.tb01087.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  11 in total

1.  Dermatology: recessive x-linked ichthyosis.

Authors:  M L Williams
Journal:  West J Med       Date:  1985-08

2.  Hexanol dehydrogenase activity shown by enzyme histochemistry on skin biopsies allows differentiation of Sjögren-Larsson syndrome from other ichthyoses.

Authors:  B D Lake; V V Smith; M R Judge; J I Harper; G T Besley
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

3.  Keratohyalin granules are heterogeneous in ridged and non-ridged human skin: evidence from anti-filaggrin immunogold labelling of normal skin and skin of autosomal dominant ichthyosis vulgaris patients.

Authors:  S Günzel; B Weidenthaler; I Hausser; I Anton-Lamprecht
Journal:  Arch Dermatol Res       Date:  1991       Impact factor: 3.017

4.  Prenatal diagnosis of bullous ichthyosiform erythroderma: detection of tonofilament clumps in fetal epidermal and amniotic fluid cells.

Authors:  R A Eady; D B Gunner; L D Carbone; F D Bricarelli; C M Gosden; C H Rodeck
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

5.  Cholesterol sulphate in the microsomal sulphatase deficient placenta.

Authors:  A Marinkovic-Ilsen; M L Williams
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

6.  Ichthyosis congenita type III. Clinical and ultrastructural characteristics and distinction within the heterogeneous ichthyosis congenita group.

Authors:  M L Arnold; I Anton-Lamprecht; B Melz-Rothfuss; W Hartschuh
Journal:  Arch Dermatol Res       Date:  1988       Impact factor: 3.017

7.  Human stratum corneum polar lipids and desquamation.

Authors:  S A Long; P W Wertz; J S Strauss; D T Downing
Journal:  Arch Dermatol Res       Date:  1985       Impact factor: 3.017

8.  Elevated n-alkanes in congenital ichthyosiform erythroderma. Phenotypic differentiation of two types of autosomal recessive ichthyosis.

Authors:  M L Williams; P M Elias
Journal:  J Clin Invest       Date:  1984-07       Impact factor: 14.808

9.  Gene diagnosis in X-linked ichthyosis.

Authors:  F H Herrmann; B Wirth; K Wulff; J Hadlich; M Voss; E F Gillard; T A Kruse; M A Ferguson-Smith; A Gal
Journal:  Arch Dermatol Res       Date:  1989       Impact factor: 3.017

10.  Problems in prenatal diagnosis of the ichthyosis congenita group.

Authors:  M L Arnold; I Anton-Lamprecht
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

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