Comparison of the clinical phenotype and haematological course of siblings with Fanconi anaemia Journal Article


Authors: Jung, M.; Mehta, P. A.; Jiang, C. S.; Rosti, R. O.; Usleaman, G.; Correa da Rosa, J. M.; Lach, F. P.; Goodridge, E.; Auerbach, A. D.; Davies, S. M.; Smogorzewska, A.; Boulad, F.
Article Title: Comparison of the clinical phenotype and haematological course of siblings with Fanconi anaemia
Abstract: Fanconi anaemia (FA) is a genetic disorder due to mutations in any of the 22 FANC genes (FANCA–FANCW) and has high phenotypic variation. Siblings may have similar clinical outcome because they share the same variants; however, such association has not been reported. We present the detailed phenotype and clinical course of 25 sibling sets with FA from two institutions. Haematological progression significantly correlated between siblings, which was confirmed in an additional 55 sibling pairs from the International Fanconi Anemia Registry. Constitutional abnormalities were not concordant, except for a moderate degree of concordance in kidney abnormalities and microcephaly. © 2020 British Society for Haematology and John Wiley & Sons Ltd
Keywords: sibling; fanconi anemia; aml; mds; bone marrow failure; prognosis
Journal Title: British Journal of Haematology
Volume: 193
Issue: 5
ISSN: 0007-1048
Publisher: John Wiley & Sons  
Date Published: 2021-06-01
Start Page: 971
End Page: 975
Language: English
DOI: 10.1111/bjh.17061
PUBMED: 32866285
PROVIDER: scopus
PMCID: PMC7914271
DOI/URL:
Notes: Article -- Export Date: 1 July 2021 -- Source: Scopus
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  1. Farid Boulad
    329 Boulad