A unique LAMB3 splice‐site mutation with founder effect from the Balkans causes lethal epidermolysis bullosa in several European countries. (1st October 2016)

• Record Type: Journal Article
• Authors: Mayer, B.; Silló, P.; Mazán, M.; Pintér, D.; Medvecz, M.; Has, C.; Castiglia, D.; Petit, F.; Charlesworth, A.; Hatvani, Zs.; Pamjav, H.; Kárpáti, S.
• Is Part Of: British journal of dermatology. Volume 175:Number 4(2016)
• Page Start: 721
• Page End: 727
• Publication Date: 2016-10-01
• Subjects: Dermatology -- Periodicals; Skin -- Diseases -- Periodicals; 616.5
• DOI: 10.1111/bjd.14646
• Languages: English
• ISSNs: 0007-0963

Abstract

Summary: Background: We have encountered repeated cases of recessive lethal generalized severe (Herlitz‐type) junctional epidermolysis bullosa (JEB gen sev) in infants born to Hungarian Roma parents residing in a small region of Hungary. Objectives: To identify the disease‐causing mutation and to investigate the genetic background of its unique carrier group. Methods: The LAMB3 gene was analysed in peripheral‐blood genomic DNA samples, and the pathological consequences of the lethal defect were confirmed by cutaneous LAMB3 cDNA sequencing. A median joining haplotype network within the Y chromosome H1a‐M82 haplogroup of individuals from the community was constructed, and LAMB3 single‐nucleotide polymorphism (SNP) patterns were also determined. Results: An unconventional intronic splice‐site mutation ( LAMB3, c.1133–22G>A) was identified. Thirty of 64 voluntarily screened Roma from the closed community carried the mutation, but none of the 306 Roma from other regions of the country did. The age of the mutation was estimated to be 548 ± 222 years. Within the last year, more patients with JEB gen sev carrying the same unusual mutation have been identified in three unrelated families, all immigrants from the Balkans. Two were compound heterozygous newborns, in Germany and Italy, and one homozygous newborn died in France. Only the French family recognized their Roma background. LAMB3 SNP haplotyping confirmed the link between the apparently unrelated Hungarian, German and Italian male cases, but could not verify the same background in the female newborn from France. Conclusions: The estimated age of the mutation corresponds to the time period when Roma were wandering in the Balkans.