Epidermolysis bullosa simplex with PLEC mutations: New phenotypes and new mutations

A. Charlesworth, C. Chiaverini, J. Chevrant-Breton, M. Delrio, A. Diociaiuti, R. P. Dupuis, M. El Hachem, B. Le Fiblec, A. M. Sankari-Ho, A. Valhquist, E. Wierzbicka, J. P. Lacour, G. Meneguzzi

Research output: Contribution to journalArticle

Abstract

Background Genetic mutations in the plectin gene (PLEC) cause autosomal recessive forms of epidermolysis bullosa simplex (EBS) associated with either muscular dystrophy (EBS-MD) or pyloric atresia (EBS-PA). Phenotype-genotype analysis has suggested that EBS-MD is due mostly to genetic mutations affecting the central rod domain of plectin, and EBS-PA to mutations outside this domain. Objectives This study aimed to describe new phenotypes of patients with EBS-MD and EBS-PA, to identify novel PLEC mutations and to establish genotype-phenotype correlations. Methods Seven patients with a suspicion of EBS linked to PLEC mutations were included. A standardized clinical questionnaire was sent to the physicians in charge of each patient. Immunofluorescence studies of skin biopsies followed by molecular analysis of PLEC were performed in all patients. Results We report the first case of nonlethal EBS-PA improving with age, the first multisystemic involvement in a patient with lethal EBS-PA, and the first patients with EBS-MD with involvement of either the bladder or oesophagus. Eleven novel PLEC mutations are also reported. Conclusions Our results confirm that EBS-PA is linked to mutations in the distal exons 1-30 and 32 of PLEC. Long-term survival is possible, with skin improvement, but a delayed onset of MD is probable. While EBS-MD is linked to PLEC mutations in all exons, in most cases one of the mutations affects exon 31. The precocity of MD seems to be linked to the type and localization of the PLEC mutation(s), but no correlation with mucosal involvement has been found.

Original languageEnglish
Pages (from-to)808-814
Number of pages7
JournalBritish Journal of Dermatology
Volume168
Issue number4
DOIs
Publication statusPublished - Apr 2013

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Plectin
Epidermolysis Bullosa Simplex
Phenotype
Mutation
Genes
Exons
Skin
Genetic Association Studies
Esophagus
Fluorescent Antibody Technique
Urinary Bladder

ASJC Scopus subject areas

  • Dermatology

Cite this

Charlesworth, A., Chiaverini, C., Chevrant-Breton, J., Delrio, M., Diociaiuti, A., Dupuis, R. P., ... Meneguzzi, G. (2013). Epidermolysis bullosa simplex with PLEC mutations: New phenotypes and new mutations. British Journal of Dermatology, 168(4), 808-814. https://doi.org/10.1111/bjd.12202

Epidermolysis bullosa simplex with PLEC mutations : New phenotypes and new mutations. / Charlesworth, A.; Chiaverini, C.; Chevrant-Breton, J.; Delrio, M.; Diociaiuti, A.; Dupuis, R. P.; El Hachem, M.; Le Fiblec, B.; Sankari-Ho, A. M.; Valhquist, A.; Wierzbicka, E.; Lacour, J. P.; Meneguzzi, G.

In: British Journal of Dermatology, Vol. 168, No. 4, 04.2013, p. 808-814.

Research output: Contribution to journalArticle

Charlesworth, A, Chiaverini, C, Chevrant-Breton, J, Delrio, M, Diociaiuti, A, Dupuis, RP, El Hachem, M, Le Fiblec, B, Sankari-Ho, AM, Valhquist, A, Wierzbicka, E, Lacour, JP & Meneguzzi, G 2013, 'Epidermolysis bullosa simplex with PLEC mutations: New phenotypes and new mutations', British Journal of Dermatology, vol. 168, no. 4, pp. 808-814. https://doi.org/10.1111/bjd.12202
Charlesworth, A. ; Chiaverini, C. ; Chevrant-Breton, J. ; Delrio, M. ; Diociaiuti, A. ; Dupuis, R. P. ; El Hachem, M. ; Le Fiblec, B. ; Sankari-Ho, A. M. ; Valhquist, A. ; Wierzbicka, E. ; Lacour, J. P. ; Meneguzzi, G. / Epidermolysis bullosa simplex with PLEC mutations : New phenotypes and new mutations. In: British Journal of Dermatology. 2013 ; Vol. 168, No. 4. pp. 808-814.
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abstract = "Background Genetic mutations in the plectin gene (PLEC) cause autosomal recessive forms of epidermolysis bullosa simplex (EBS) associated with either muscular dystrophy (EBS-MD) or pyloric atresia (EBS-PA). Phenotype-genotype analysis has suggested that EBS-MD is due mostly to genetic mutations affecting the central rod domain of plectin, and EBS-PA to mutations outside this domain. Objectives This study aimed to describe new phenotypes of patients with EBS-MD and EBS-PA, to identify novel PLEC mutations and to establish genotype-phenotype correlations. Methods Seven patients with a suspicion of EBS linked to PLEC mutations were included. A standardized clinical questionnaire was sent to the physicians in charge of each patient. Immunofluorescence studies of skin biopsies followed by molecular analysis of PLEC were performed in all patients. Results We report the first case of nonlethal EBS-PA improving with age, the first multisystemic involvement in a patient with lethal EBS-PA, and the first patients with EBS-MD with involvement of either the bladder or oesophagus. Eleven novel PLEC mutations are also reported. Conclusions Our results confirm that EBS-PA is linked to mutations in the distal exons 1-30 and 32 of PLEC. Long-term survival is possible, with skin improvement, but a delayed onset of MD is probable. While EBS-MD is linked to PLEC mutations in all exons, in most cases one of the mutations affects exon 31. The precocity of MD seems to be linked to the type and localization of the PLEC mutation(s), but no correlation with mucosal involvement has been found.",
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AU - Charlesworth, A.

AU - Chiaverini, C.

AU - Chevrant-Breton, J.

AU - Delrio, M.

AU - Diociaiuti, A.

AU - Dupuis, R. P.

AU - El Hachem, M.

AU - Le Fiblec, B.

AU - Sankari-Ho, A. M.

AU - Valhquist, A.

AU - Wierzbicka, E.

AU - Lacour, J. P.

AU - Meneguzzi, G.

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Y1 - 2013/4

N2 - Background Genetic mutations in the plectin gene (PLEC) cause autosomal recessive forms of epidermolysis bullosa simplex (EBS) associated with either muscular dystrophy (EBS-MD) or pyloric atresia (EBS-PA). Phenotype-genotype analysis has suggested that EBS-MD is due mostly to genetic mutations affecting the central rod domain of plectin, and EBS-PA to mutations outside this domain. Objectives This study aimed to describe new phenotypes of patients with EBS-MD and EBS-PA, to identify novel PLEC mutations and to establish genotype-phenotype correlations. Methods Seven patients with a suspicion of EBS linked to PLEC mutations were included. A standardized clinical questionnaire was sent to the physicians in charge of each patient. Immunofluorescence studies of skin biopsies followed by molecular analysis of PLEC were performed in all patients. Results We report the first case of nonlethal EBS-PA improving with age, the first multisystemic involvement in a patient with lethal EBS-PA, and the first patients with EBS-MD with involvement of either the bladder or oesophagus. Eleven novel PLEC mutations are also reported. Conclusions Our results confirm that EBS-PA is linked to mutations in the distal exons 1-30 and 32 of PLEC. Long-term survival is possible, with skin improvement, but a delayed onset of MD is probable. While EBS-MD is linked to PLEC mutations in all exons, in most cases one of the mutations affects exon 31. The precocity of MD seems to be linked to the type and localization of the PLEC mutation(s), but no correlation with mucosal involvement has been found.

AB - Background Genetic mutations in the plectin gene (PLEC) cause autosomal recessive forms of epidermolysis bullosa simplex (EBS) associated with either muscular dystrophy (EBS-MD) or pyloric atresia (EBS-PA). Phenotype-genotype analysis has suggested that EBS-MD is due mostly to genetic mutations affecting the central rod domain of plectin, and EBS-PA to mutations outside this domain. Objectives This study aimed to describe new phenotypes of patients with EBS-MD and EBS-PA, to identify novel PLEC mutations and to establish genotype-phenotype correlations. Methods Seven patients with a suspicion of EBS linked to PLEC mutations were included. A standardized clinical questionnaire was sent to the physicians in charge of each patient. Immunofluorescence studies of skin biopsies followed by molecular analysis of PLEC were performed in all patients. Results We report the first case of nonlethal EBS-PA improving with age, the first multisystemic involvement in a patient with lethal EBS-PA, and the first patients with EBS-MD with involvement of either the bladder or oesophagus. Eleven novel PLEC mutations are also reported. Conclusions Our results confirm that EBS-PA is linked to mutations in the distal exons 1-30 and 32 of PLEC. Long-term survival is possible, with skin improvement, but a delayed onset of MD is probable. While EBS-MD is linked to PLEC mutations in all exons, in most cases one of the mutations affects exon 31. The precocity of MD seems to be linked to the type and localization of the PLEC mutation(s), but no correlation with mucosal involvement has been found.

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