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Diamond-Blackfan anemia caused by chromosome 1p22 deletion encompassing RPL5
Makiko Tominaga1,2, Satoshi Hamanoue3, Hiroaki Goto3
11Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
Abstract:
Diamond-Blackfan anemia (DBA) is an inherited anemia with multiple congenital malformations, and mutations in ribosomal protein genes have been identified as the underlying cause. We describe a female patient with mild DBA due to 1p22 deletion, encompassing the gene encoding 60S ribosomal protein L5 (RPL5). Considering previously reported cases together with our patient, we suggest that RPL5 haploinsufficiency might cause a less severe form of DBA than loss-of-function mutations.
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