Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations

Mordechai Mizrachi-Koren, Saar Shemer, Michal Morgan, Margarita Indelman, Ziad Khamaysi, Danny Petronius, Ora Bitterman-Deutsch, Hans Christian Hennies, Reuven Bergman, Eli Sprecher

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Background: The routine diagnosis of genodermatoses is significantly complicated by the fact that in this group of disorders, clinical manifestations may result from mutations in unrelated genes (genetic heterogeneity) and mutations in the same gene often lead to dissimilar clinical signs (phenotypic heterogeneity). Methods: In this study, we applied the principles of homozygosity mapping as a screening method before formal mutational analysis in an attempt to facilitate the molecular diagnosis of genodermatoses in consanguineous families. The method was evaluated in a retrospective fashion in 4 families previously assessed with junctional epidermolysis bullosa and in a prospective manner in 11 families with congenital recessive ichthyosis. Results: The method was found to be efficient in directing the molecular analysis to one of the 4 genes commonly involved in the pathogenesis of junctional epidermolysis bullosa or in identifying cases of congenital recessive ichthyosis caused by mutations in TGM1. We found that this diagnostic strategy results in a 5-fold decrease in the cost of mutation analysis. Limitations: The proposed diagnostic strategy is applicable to consanguineous families only and, therefore, cannot be used in outbred populations. Conclusion: Our results indicate that homozygosity mapping may serve as a useful adjunct in the molecular diagnosis of junctional epidermolysis bullosa or congenital recessive ichthyosis in inbred populations. This study emphasizes the usefulness in human genetics of diagnostic strategies tailored to the demographic features of target populations.

Original languageEnglish
Pages (from-to)393-401
Number of pages9
JournalJournal of the American Academy of Dermatology
Volume55
Issue number3
DOIs
Publication statusPublished - 1 Sep 2006
Externally publishedYes

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Inborn Genetic Diseases
Junctional Epidermolysis Bullosa
Ichthyosis
Skin Diseases
Mutation
Population
Genes
Genetic Heterogeneity
Health Services Needs and Demand
Medical Genetics
Demography
Costs and Cost Analysis

Cite this

Mizrachi-Koren, Mordechai ; Shemer, Saar ; Morgan, Michal ; Indelman, Margarita ; Khamaysi, Ziad ; Petronius, Danny ; Bitterman-Deutsch, Ora ; Hennies, Hans Christian ; Bergman, Reuven ; Sprecher, Eli. / Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations. In: Journal of the American Academy of Dermatology. 2006 ; Vol. 55, No. 3. pp. 393-401.
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Mizrachi-Koren, M, Shemer, S, Morgan, M, Indelman, M, Khamaysi, Z, Petronius, D, Bitterman-Deutsch, O, Hennies, HC, Bergman, R & Sprecher, E 2006, 'Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations', Journal of the American Academy of Dermatology, vol. 55, no. 3, pp. 393-401. https://doi.org/10.1016/j.jaad.2006.02.020

Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations. / Mizrachi-Koren, Mordechai; Shemer, Saar; Morgan, Michal; Indelman, Margarita; Khamaysi, Ziad; Petronius, Danny; Bitterman-Deutsch, Ora; Hennies, Hans Christian; Bergman, Reuven; Sprecher, Eli.

In: Journal of the American Academy of Dermatology, Vol. 55, No. 3, 01.09.2006, p. 393-401.

Research output: Contribution to journalArticle

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T1 - Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations

AU - Mizrachi-Koren, Mordechai

AU - Shemer, Saar

AU - Morgan, Michal

AU - Indelman, Margarita

AU - Khamaysi, Ziad

AU - Petronius, Danny

AU - Bitterman-Deutsch, Ora

AU - Hennies, Hans Christian

AU - Bergman, Reuven

AU - Sprecher, Eli

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N2 - Background: The routine diagnosis of genodermatoses is significantly complicated by the fact that in this group of disorders, clinical manifestations may result from mutations in unrelated genes (genetic heterogeneity) and mutations in the same gene often lead to dissimilar clinical signs (phenotypic heterogeneity). Methods: In this study, we applied the principles of homozygosity mapping as a screening method before formal mutational analysis in an attempt to facilitate the molecular diagnosis of genodermatoses in consanguineous families. The method was evaluated in a retrospective fashion in 4 families previously assessed with junctional epidermolysis bullosa and in a prospective manner in 11 families with congenital recessive ichthyosis. Results: The method was found to be efficient in directing the molecular analysis to one of the 4 genes commonly involved in the pathogenesis of junctional epidermolysis bullosa or in identifying cases of congenital recessive ichthyosis caused by mutations in TGM1. We found that this diagnostic strategy results in a 5-fold decrease in the cost of mutation analysis. Limitations: The proposed diagnostic strategy is applicable to consanguineous families only and, therefore, cannot be used in outbred populations. Conclusion: Our results indicate that homozygosity mapping may serve as a useful adjunct in the molecular diagnosis of junctional epidermolysis bullosa or congenital recessive ichthyosis in inbred populations. This study emphasizes the usefulness in human genetics of diagnostic strategies tailored to the demographic features of target populations.

AB - Background: The routine diagnosis of genodermatoses is significantly complicated by the fact that in this group of disorders, clinical manifestations may result from mutations in unrelated genes (genetic heterogeneity) and mutations in the same gene often lead to dissimilar clinical signs (phenotypic heterogeneity). Methods: In this study, we applied the principles of homozygosity mapping as a screening method before formal mutational analysis in an attempt to facilitate the molecular diagnosis of genodermatoses in consanguineous families. The method was evaluated in a retrospective fashion in 4 families previously assessed with junctional epidermolysis bullosa and in a prospective manner in 11 families with congenital recessive ichthyosis. Results: The method was found to be efficient in directing the molecular analysis to one of the 4 genes commonly involved in the pathogenesis of junctional epidermolysis bullosa or in identifying cases of congenital recessive ichthyosis caused by mutations in TGM1. We found that this diagnostic strategy results in a 5-fold decrease in the cost of mutation analysis. Limitations: The proposed diagnostic strategy is applicable to consanguineous families only and, therefore, cannot be used in outbred populations. Conclusion: Our results indicate that homozygosity mapping may serve as a useful adjunct in the molecular diagnosis of junctional epidermolysis bullosa or congenital recessive ichthyosis in inbred populations. This study emphasizes the usefulness in human genetics of diagnostic strategies tailored to the demographic features of target populations.

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