Biallelic variants inDNA2cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome

Author:

Di Lazzaro Filho Ricardo,Yamamoto Guilherme Lopes,Silva Tiago J,Rocha Leticia A,Linnenkamp Bianca D W,Castro Matheus Augusto AraújoORCID,Bartholdi Deborah,Schaller AndréORCID,Leeb Tosso,Kelmann Samantha,Utagawa Claudia Y,Steiner Carlos E,Steinmetz Leandra,Honjo Rachel Sayuri,Kim Chong Ae,Wang Lisa,Abourjaili-Bilodeau Raphaël,Campeau Philippe MORCID,Warman MatthewORCID,Passos-Bueno Maria Rita,Hoch Nicolas C,Bertola Debora RomeoORCID

Abstract

Rothmund-Thomson syndrome (RTS) is a rare, heterogeneous autosomal recessive genodermatosis, with poikiloderma as its hallmark. It is classified into two types: type I, with biallelic variants inANAPC1and juvenile cataracts, and type II, with biallelic variants inRECQL4, increased cancer risk and no cataracts. We report on six Brazilian probands and two siblings of Swiss/Portuguese ancestry presenting with severe short stature, widespread poikiloderma and congenital ocular anomalies. Genomic and functional analysis revealed compound heterozygosis for a deep intronic splicing variant in trans with loss of function variants inDNA2, with reduction of the protein levels and impaired DNA double-strand break repair. The intronic variant is shared by all patients, as well as the Portuguese father of the European siblings, indicating a probable founder effect. Biallelic variants inDNA2were previously associated with microcephalic osteodysplastic primordial dwarfism. Although the individuals reported here present a similar growth pattern, the presence of poikiloderma and ocular anomalies is unique. Thus, we have broadened the phenotypical spectrum ofDNA2mutations, incorporating clinical characteristics of RTS. Although a clear genotype–phenotype correlation cannot be definitively established at this moment, we speculate that the residual activity of the splicing variant allele could be responsible for the distinct manifestations ofDNA2-related syndromes.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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