Diagnostic challenge of Diamond–Blackfan anemia in mothers and children by whole-exome sequencing

• Published in: International journal of hematology Vol. 105; no. 4; pp. 515 - 520
• Main Authors: Ichimura, Takuya, Yoshida, Kenichi, Okuno, Yusuke, Yujiri, Toshiaki, Nagai, Kozo, Nishi, Masanori, Shiraishi, Yuichi, Ueno, Hiroo, Toki, Tsutomu, Chiba, Kenichi, Tanaka, Hiroko, Muramatsu, Hideki, Hara, Toshiro, Kanno, Hitoshi, Kojima, Seiji, Miyano, Satoru, Ito, Etsuro, Ogawa, Seishi, Ohga, Shouichi
• Format: Journal Article
• Language: English
• Published: Tokyo Springer Japan 01.04.2017; Springer Nature B.V
• Subjects: Abnormalities, Multiple - genetics; Adult; Anemia, Diamond-Blackfan - diagnosis; Anemia, Diamond-Blackfan - genetics; Child, Preschool; Exome - genetics; Facies; Family; Female; Hematology; Humans; Male; Medicine; Medicine & Public Health; Muscular Atrophy - genetics; Oncology; Original Article; Pedigree; Ribosomal Proteins - genetics; Sequence Analysis, DNA; Inherited bone marrow failure syndrome; Ribosomal protein; Diamond–Blackfan anemia; Whole-exome sequencing
• ISSN: 0925-5710; 1865-3774
• DOI: 10.1007/s12185-016-2151-7

Diamond–Blackfan anemia (DBA) is a pure red cell aplasia that arises from defective ribosomal proteins (RPs). Patients with this rare ribosomopathy present with neonatal anemia and occasional dysmorphism. Clinical heterogeneity and clusters of causative RP genes hamper the diagnosis and perinatal management. We report three mother-and-child pairs of anemia who were finally diagnosed by whole-exome sequencing. Each pair showed distinct disease severity and response to anemia treatment. Only one mother had the diagnostic dysmorphism, including short stature, webbed neck, and thenar hypoplasia. This mother had a frame-shift mutation of RPL11 (exon 3, c.58_59del). Her infant showed transient neonatal anemia, but had no mutations of RP genes. The other mother–child pairs had a missense mutation of RPS19 (exon 4, c.185G>A), and a splicing error of RPS7 (exon 3, c.76-1G>T), respectively. Other than the reported mutations, there were no variants in genes significantly associated with anemia. Our results suggested that whole-exome sequencing (WES) is effective for achieving a prompt and correct diagnosis of human ribosomopathy.