RPL26 variants: a rare cause of Diamond-Blackfan Anemia Syndrome with multiple congenital anomalies at the forefront.
Genet Med
; : 101266, 2024 Sep 10.
Article
en En
| MEDLINE
| ID: mdl-39268718
ABSTRACT
PURPOSE:
Diamond-Blackfan Anemia Syndrome (DBS) is a rare congenital disorder originally characterized by bone marrow failure with or without various congenital anomalies. At least 24 genes are implicated, the vast majority encoding for ribosomal proteins. RPL26 (ribosomal protein L26) is an emerging candidate (DBA11, MIM#614900). We aim to further delineate this rare condition.METHODS:
Patients carrying heterozygous RPL26 variants were recruited. In one of them, erythroid proliferation and differentiation from peripheral blood CD34+ cells were studied by flow cytometry, and RPL26 expression by qRT-PCR and immunoblotting.RESULTS:
We report on eight affected patients from four families. Detailed phenotyping reveals that RPL26 is mainly associated with multiple congenital anomalies (particularly radial ray anomalies), albeit with variable expression. Mandibulofacial dysostosis and neural tube defects are potential features in DBA11, expanding the growing list of DBS abnormalities. In one individual, we showed that RPL26 haploinsufficiency was responsible for subclinical impairment in erythroid proliferation and enucleation. The absence of hematological involvement in four adults from this series contributes to the mounting evidence that bone marrow failure is not universally central to all DBS genes.CONCLUSION:
We confirm RPL26 as a DBS gene and expand the phenotypic spectrum of the gene and the disease.
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Colección:
01-internacional
Base de datos:
MEDLINE
Idioma:
En
Revista:
Genet Med
Asunto de la revista:
GENETICA MEDICA
Año:
2024
Tipo del documento:
Article
Pais de publicación:
Estados Unidos