Cases of Ichthyosis Spuria Vel Sebacea
نویسندگان
چکیده
منابع مشابه
Harlequin Ichthyosis: A report of two cases
Harlequin ichthyosis is one of the most severe congenital skin cornification disorders with an incidence rate of about 1 in 300000 births and characteristic clinical features. We report two cases of harlequin ichthyosis (HI) or harlequin fetus (HF), which were products of consanguineous union. Clinical examination showed typical features of harlequin ichthyosis, with the presence of plaques wit...
متن کاملIchthyosis associated with widespread tinea corporis: report of three cases*
Ichthyoses are a common group of keratinization disorders. A non-inflammatory generalized persistent skin desquamation is observed. It is characterized by increased cell turnover, thickening of the stratum corneum and functional changes of sebaceous and sweat glands. All of these favor fungal proliferation. Dermatophytes may infect skin, hair and nails causing ringworm or tinea. They have the a...
متن کاملLamellar ichthyosis is genetically heterogeneous--cases with normal keratinocyte transglutaminase.
We recently identified mutations of the keratinocyte transglutaminase gene as a cause of lamellar ichthyosis. In this study we analyzed two sporadic cases of lamellar ichthyosis. Transglutaminase activity measured in membrane extracts from cultured differentiating keratinocytes was within the range observed in normal individuals. Western blot and Northern blot analysis revealed normal size and ...
متن کاملReport of a Congenital Ichthyosis
A case of congenital ichthiosis 1s presented. Histologic pattern and the treatment is discussed.
متن کاملa report of two cases of tgm1 mutations in iranian patients with lamelar ichthyosis
objective autosomal recessive congenital ichthyosis (arci) is a rare, heterogenous keratinization disorder of the skin, classically divided into two clinical subtypes, lamellar ichthyosis (li) and nonbullous congenital ichthyosi-formis erythroderma (ncie). lamellar ichtyosis is caused by mutations in the tgm1 gene that encodes transglutaminase 1 enzyme, which is critical for the assembly of the...
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ژورنال
عنوان ژورنال: Journal of the Royal Society of Medicine
سال: 1863
ISSN: 0959-5287,1758-1095
DOI: 10.1177/095952876304600121