[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.205.87.3. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
November 1993

Harlequin IchthyosisVariability in Expression and Hypothesis for Disease Mechanism

Author Affiliations

From the Departments of Oral Biology, Periodontics, Medicine/Dermatology, and Biochemistry, University of Washington, Seattle.

Arch Dermatol. 1993;129(11):1471-1477. doi:10.1001/archderm.1993.01680320105014
Abstract

Background:  Harlequin ichthyosis is an inherited skin disorder that usually results in death shortly after birth. Although the clinical features of this disorder are well described, the underlying molecular basis is not understood. In this article, we discuss the results of the latest histologic, immunochemical, and Western immunoblotting studies done in our laboratory and propose a hypothesis for molecular basis of this disorder.

Observations:  Previous experiments done in our laboratory show suggestive evidence for defective lipid synthesis and protein dephosphorylation in harlequin ichthyosis. Our latest study shows that the catalytic subunit of one of the most prevalent protein phosphatase, type 2A protein phosphatase, appears to be altered in some cases of type 2 harlequin ichthyosis.

Conclusions:  Based on these observations and the known functions of protein phosphatase in keratinocytes, we hypothesize that the underlying molecular basis of harlequin ichthyosis may be related to mutations affecting protein dephosphorylation. We further describe approaches by which this hypothesis can be tested.(Arch Dermatol. 1993;129:1471-1477)

×