[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.204.247.205. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
September 1992

Peroxisomal Abnormality in Fibroblasts From Involved Skin of CHILD SyndromeCase Study and Review of Peroxisomal Disorders in Relation to Skin Disease

Author Affiliations

From the Departments of Dermatology (Drs Emami, Goldyne, and Williams and Ms Hanley), Medicine (Dr Goldyne) and Pediatrics (Dr Williams), University of California, San Francisco; the Dermatology Service, Veterans Administration Medical Center, San Francisco (Drs Emami, Goldyne, and Williams and Ms Hanley); the Departments of Pediatrics and Genetics, Medical College of Virginia, Virginia Commonwealth University, Richmond (Dr Rizzo); and the Maine Medical Center, Portland (Dr Taylor).

Arch Dermatol. 1992;128(9):1213-1222. doi:10.1001/archderm.1992.01680190069008
Abstract

• Background and Design.—  Peroxisomal deficiency has been described in a number of syndromes characterized by chondrodysplasia punctata, including the Conradi-Hünermann (C-H) syndrome. Because of overlapping clinical features of X-chromosome inheritance, ichthyosis, and limbreduction defects in C-H and CHILD (congenital hemidysplasia with ichthyosiform erythroderma and limb defects) syndromes, we examined peroxisomal content using diaminobenzidine cytochemistry and peroxisomal functions in fibroblasts from involved vs uninvolved skin of CHILD syndrome.

Results.—  Fibroblasts from involved skin of a patient with CHILD syndrome accumulated cytoplasmic lipid, visualized with the fluorescent probe, nile-red. Ultrastructurally, fibroblasts of involved skin of CHILD syndrome accumulated lamellated membrane and vacuolar structures. By diaminobenzidine ultracytochemistry, fewer peroxisomes were present. Moreover, the activities of two peroxisomal enzymes, catalase and dihydroxyacetone phosphate acyltransferase, were decreased (approximately 30% of normal). However, peroxisomal oxidation of very-long-chain and branched-chain fatty acids was preserved. Moreover, plasma very-long-chain fatty acids, plasma phytanic acid, and erythrocyte plasmalogen content were normal.

Conclusions.—  The CHILD, C-H, and rhizomelic chondrodysplasia punctata syndromes are all characterized by ichthyosis, chondrodysplasia punctata, and limb defects, as well as peroxisomal deficiency. Thus, these syndromes may be related pathogenically. Because peroxisomes are involved in prostaglandin metabolism, peroxisomal deficiency may directly contribute to the previously reported alterations in prostaglandin metabolism in fibroblasts of involved skin of fibroblasts.(Arch Dermatol. 1992;128:1213-1222)

×