# Editorial: Recent advances in pediatric red blood cells disorders

**Authors:** Gabriele Canciani, Giuseppe Palumbo, John Brewin, Francesca Rossi, Giulia Ceglie

PMC · DOI: 10.3389/fped.2024.1403651 · Frontiers in Pediatrics · 2024-04-03

## Full-text entities

- **Genes:** BCL11A (BCL11 transcription factor A) [NCBI Gene 53335] {aka CTIP1, DILOS, EVI9, HBFQTL5, SMARCM1, ZNF856}, SLC30A10 (solute carrier family 30 member 10) [NCBI Gene 55532] {aka HMDPC, HMNDYT1, ZNT10, ZNT8, ZRC1, ZnT-10}, GCA (grancalcin) [NCBI Gene 25801] {aka GCL}, HBG1 (hemoglobin subunit gamma 1) [NCBI Gene 3047] {aka HBG-T2, HBGA, HBGR, HSGGL1, PRO2979}
- **Diseases:** SCD (MESH:D000755), erythrocytes (MESH:D012010), thalassemias (MESH:D013789), erythrocytosis (MESH:D011086), iron deficiency anemia (MESH:D018798), abnormalities (MESH:D000014), viral infections (MESH:D014777), anemia (MESH:D000740), RBC disorders (MESH:C562718), alternative complement pathways disorders (MESH:C536589), monogenic diseases (MESH:D004194), beta-thalassemia (MESH:D017086), parkinsonism (MESH:D010302), neurodegeneration (MESH:D019636), hemolytic anemia (MESH:D000743), Hemoglobinopathies (MESH:D006453), hepatobiliary disorders (MESH:D004066), HS (MESH:C567159), AIHA (MESH:D000744), genetic diseases (MESH:D030342), HMNDYT1 (MESH:D004421)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC11021739/full.md

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Source: https://tomesphere.com/paper/PMC11021739