HUSCAP logo Hokkaido Univ. logo

Hokkaido University Collection of Scholarly and Academic Papers >
Hokkaido University Hospital >
Peer-reviewed Journal Articles, etc >

Harlequin ichthyosis and other autosomal recessive congenital ichthyoses : The underlying genetic defects and pathomechanisms

Files in This Item:
main.pdf795.29 kBPDFView/Open
Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/13466

Title: Harlequin ichthyosis and other autosomal recessive congenital ichthyoses : The underlying genetic defects and pathomechanisms
Authors: Akiyama, Masashi1 Browse this author
Authors(alt): 秋山, 真志1
Keywords: ABCA12
Prenatal diagnosis
Harlequin ichthyosis
Lamellar granules
Lamellar ichthyosis
Non-bullous congenital ichthyosiform erythroderma
Issue Date: May-2006
Publisher: Elsevier
Journal Title: Journal of Dermatological Science
Volume: 42
Issue: 2
Start Page: 83
End Page: 89
Publisher DOI: 10.1016/j.jdermsci.2006.01.003
PMID: 16481150
Abstract: Autosomal recessive congenital ichthyoses (ARCI) include several severe subtypes including harlequin ichthyosis (HI), lamellar ichthyosis and non-bullous congenital ichthyosiform erythroderma. Patients with these severe types of ichthyoses frequently show severe hyperkeratosis and scales over a large part of the body surface form birth and their quality of life is often severely affected. Recently, research into the pathomechanisms of these severe congenital ichthyoses have advanced dramatically and led to the identification of several causative genes and molecules underlying the genetic defects. To date, seven loci have been identified that are associated with ARCI and, among them, five causative genes and molecules have been detected. The five genes are transglutaminase 1 gene (TGM1), ABCA12, two lipoxygenase genes, ALOXE3 and ALOX12B and ichthyin. One of these components, ABCA12, has recently been shown to be a keratinocyte lipid transporter associated with lipid transport in lamellar granules and loss of ABCA12 function leads to a defective lipid barrier in the stratum corneum, resulting in the HI phenotype. Transglutaminse 1 deficiency was reported to cause a malformed cornified cell envelope leading to a defect in the intercellular lipid layers in the stratum corneum and defective stratum corneum barrier function resulting in an ichthyosis phenotype. Thus, defective intercellular lipid layers are major findings in autosomal recessive congenital ichthyoses. Information concerning ARCI genetic defects and disease pathomechanisms are beneficial for providing better treatments and genetic counseling including prenatal diagnosis for families affect by ichthyoses.
Relation: http://www.sciencedirect.com/science/journal/09231811
Type: article (author version)
URI: http://hdl.handle.net/2115/13466
Appears in Collections:北海道大学病院 (Hokkaido University Hospital) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 秋山 真志

Export metadata:

OAI-PMH ( junii2 , jpcoar )

MathJax is now OFF:


 

 - Hokkaido University