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A unique LAMB 3 splice‐site mutation with founder effect from the Balkans causes lethal epidermolysis bullosa in several European countries
Author(s) -
Mayer B.,
Silló P.,
Mazán M.,
Pintér D.,
Medvecz M.,
Has C.,
Castiglia D.,
Petit F.,
Charlesworth A.,
Hatvani Zs.,
Pamjav H.,
Kárpáti S.
Publication year - 2016
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.14646
Subject(s) - haplotype , haplogroup , epidermolysis bullosa , founder effect , junctional epidermolysis bullosa (veterinary medicine) , genetics , splice site mutation , mutation , single nucleotide polymorphism , biology , medicine , exon , allele , gene , genotype , alternative splicing
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 LAMB 3 gene was analysed in peripheral‐blood genomic DNA samples, and the pathological consequences of the lethal defect were confirmed by cutaneous LAMB 3 cDNA sequencing. A median joining haplotype network within the Y chromosome H1a‐M82 haplogroup of individuals from the community was constructed, and LAMB 3 single‐nucleotide polymorphism ( SNP ) patterns were also determined. Results An unconventional intronic splice‐site mutation ( LAMB 3 , 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. LAMB 3 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.