| Literature DB >> 26841305 |
Frank X Donovan1, Danielle C Kimble1, Yonghwan Kim2, Francis P Lach2, Ursula Harper1, Aparna Kamat1, MaryPat Jones1, Erica M Sanborn2, Rebecca Tryon3, John E Wagner3, Margaret L MacMillan3, Elaine A Ostrander1, Arleen D Auerbach4, Agata Smogorzewska2, Settara C Chandrasekharappa1.
Abstract
Fanconi anemia (FA) is a rare inherited disorder caused by pathogenic variants in one of 19 FANC genes. FA patients display congenital abnormalities, and develop bone marrow failure, and cancer susceptibility. We identified homozygous mutations in four FA patients and, in each case, only one parent carried the obligate mutant allele. FANCA and FANCP/SLX4 genes, both located on chromosome 16, were the affected recessive FA genes in three and one family respectively. Genotyping with short tandem repeat markers and SNP arrays revealed uniparental disomy (UPD) of the entire mutation-carrying chromosome 16 in all four patients. One FANCA patient had paternal UPD, whereas FA in the other three patients resulted from maternal UPD. These are the first reported cases of UPD as a cause of FA. UPD indicates a reduced risk of having another child with FA in the family and has implications in prenatal diagnosis.Entities:
Keywords: FANCA; FANCP; Fanconi anemia; Recurrence risk; UPD16; Uniparental disomy
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Year: 2016 PMID: 26841305 PMCID: PMC4833600 DOI: 10.1002/humu.22962
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878