Literature DB >> 3954411

Report of a family with an unusual expression of recessive ichthyosis. Review of 42 cases.

M Bernhardt, H P Baden.   

Abstract

A family with a history of ichthyosis is described in which the type of scale was thin and fine, resembling that of ichthyosis vulgaris, but the inheritance is of the autosomal recessive type. We have reviewed our previous experience with 42 additional patients whose condition had been diagnosed as recessively inherited ichthyosis and conclude that there is considerable heterogeneity in the cutaneous manifestations. We suggest that it is not possible to classify all patients into categories such as lamellar ichthyosis or congenital ichthyosiform erythroderma, and it may be better to use a more general term such as recessive ichthyosis until specific causes can be established.

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Year:  1986        PMID: 3954411

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  3 in total

1.  Recessive ichthyosis congenita type II.

Authors:  K M Niemi; L Kanerva; K Kuokkanen
Journal:  Arch Dermatol Res       Date:  1991       Impact factor: 3.017

2.  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

3.  Clinical, light and electron microscopic features of recessive ichthyosis congenita type III.

Authors:  K M Niemi; L Kanerva; C F Wahlgren; J Ignatius
Journal:  Arch Dermatol Res       Date:  1992       Impact factor: 3.017

  3 in total

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