Genetic and clinical mosaicism in a type of epidermal nevus

Amy S. Paller, Andrew J. Syder, Yiu Mo Chan, Qian Chun Yu, Elizabeth Hutton, Gianluca Tadini, Elaine Fuchs

Research output: Contribution to journalArticle

Abstract

Background. Many skin disorders are characterized by a mosaic pattern, often with alternating stripes of affected and unaffected skin that follow the lines of Blaschko. These nonrandom patterns may be caused by a postzygotic mutation during embryogenesis. We studied the genetic basis of one such disorder, epidermal nevus of the epidermolytic hyperkeratotic type. Epidermolytic hyperkeratosis is an autosomal dominant blistering skin disease arising from mutations in the genes for keratin (K) 1 and 10. The offspring of patients with epidermal nevi may have generalized epidermolytic hyperkeratosis. Methods. We studied the K1 and K10 genes in blood and in the keratinocytes and fibroblasts of lesional and nonlesional skin from three patients with epidermal nevi and four of their offspring with epidermolytic hyperkeratosis. Results. In the patients with epidermal nevi, point mutations in 50 percent of the K10 alleles of epidermal cells were found in keratinocytes from lesional skin; no mutations were detected in normal skin. This mutation was absent or underrepresented in blood and skin fibroblasts. In the offspring with epidermolytic hyperkeratosis, the same mutations as those in the parents were found in 50 percent of the K10 alleles from all cell types examined. Conclusions. Epidermal nevus of the epidermolytic hyperkeratotic type is a mosaic genetic disorder of supra-basal keratin. The correlation of mutations in the K10 gene with lesional skin and the correlation of the normal gene with normal skin provide evidence that genetic mosaicism can cause clinical mosaicism.

Original languageEnglish
Pages (from-to)1408-1415
Number of pages8
JournalNew England Journal of Medicine
Volume331
Issue number21
DOIs
Publication statusPublished - Nov 24 1994

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Mosaicism
Epidermolytic Hyperkeratosis
Skin
Mutation
Keratinocytes
Genes
Keratin-1
Keratin-10
Fibroblasts
Alleles
Inborn Genetic Diseases
Epidermal Nevus
Keratins
Point Mutation
Skin Diseases
Embryonic Development
Parents

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Paller, A. S., Syder, A. J., Chan, Y. M., Yu, Q. C., Hutton, E., Tadini, G., & Fuchs, E. (1994). Genetic and clinical mosaicism in a type of epidermal nevus. New England Journal of Medicine, 331(21), 1408-1415. https://doi.org/10.1056/NEJM199411243312103

Genetic and clinical mosaicism in a type of epidermal nevus. / Paller, Amy S.; Syder, Andrew J.; Chan, Yiu Mo; Yu, Qian Chun; Hutton, Elizabeth; Tadini, Gianluca; Fuchs, Elaine.

In: New England Journal of Medicine, Vol. 331, No. 21, 24.11.1994, p. 1408-1415.

Research output: Contribution to journalArticle

Paller, AS, Syder, AJ, Chan, YM, Yu, QC, Hutton, E, Tadini, G & Fuchs, E 1994, 'Genetic and clinical mosaicism in a type of epidermal nevus', New England Journal of Medicine, vol. 331, no. 21, pp. 1408-1415. https://doi.org/10.1056/NEJM199411243312103
Paller, Amy S. ; Syder, Andrew J. ; Chan, Yiu Mo ; Yu, Qian Chun ; Hutton, Elizabeth ; Tadini, Gianluca ; Fuchs, Elaine. / Genetic and clinical mosaicism in a type of epidermal nevus. In: New England Journal of Medicine. 1994 ; Vol. 331, No. 21. pp. 1408-1415.
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N2 - Background. Many skin disorders are characterized by a mosaic pattern, often with alternating stripes of affected and unaffected skin that follow the lines of Blaschko. These nonrandom patterns may be caused by a postzygotic mutation during embryogenesis. We studied the genetic basis of one such disorder, epidermal nevus of the epidermolytic hyperkeratotic type. Epidermolytic hyperkeratosis is an autosomal dominant blistering skin disease arising from mutations in the genes for keratin (K) 1 and 10. The offspring of patients with epidermal nevi may have generalized epidermolytic hyperkeratosis. Methods. We studied the K1 and K10 genes in blood and in the keratinocytes and fibroblasts of lesional and nonlesional skin from three patients with epidermal nevi and four of their offspring with epidermolytic hyperkeratosis. Results. In the patients with epidermal nevi, point mutations in 50 percent of the K10 alleles of epidermal cells were found in keratinocytes from lesional skin; no mutations were detected in normal skin. This mutation was absent or underrepresented in blood and skin fibroblasts. In the offspring with epidermolytic hyperkeratosis, the same mutations as those in the parents were found in 50 percent of the K10 alleles from all cell types examined. Conclusions. Epidermal nevus of the epidermolytic hyperkeratotic type is a mosaic genetic disorder of supra-basal keratin. The correlation of mutations in the K10 gene with lesional skin and the correlation of the normal gene with normal skin provide evidence that genetic mosaicism can cause clinical mosaicism.

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