Ontology highlight
ABSTRACT: Background
Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, short stature, congenital anomalies, and cancer predisposition. Most cases are due to mutations in genes encoding ribosomal proteins (RP) leading to RP haploinsufficiency. Effective treatments for the anemia of DBA include chronic red cell transfusions, long-term corticosteroid therapy, or hematopoietic stem cell transplantation. In a small patient series and in animal models, there have been hematologic responses to L-leucine with amelioration of anemia. The study objectives of this clinical trial were to determine feasibility, safety, and efficacy of L-leucine in transfusion-dependent patients with DBA.Procedure
Patients ≥2 years of age received L-leucine 700 mg/
SUBMITTER: Vlachos A
PROVIDER: S-EPMC8273758 | biostudies-literature | 2020 Dec
REPOSITORIES: biostudies-literature