:

Josune Zubicaray1, June Iriondo1, Elena Sebastián1

  • 1Pediatric Hematology and Oncology Department and Foundation for the Biomedical Research, and Biomedical Network Research Center for Rare Diseases (CIBERER), Pediatric University Hospital Niño Jesús, Madrid, Spain.

Frontiers in pediatrics
|August 27, 2025
PubMed
まとめ

骨髄不全症候群であるファンコニ貧血 (FA) に対して,エルトロンボパグは有望である. FAモザイク症と遺伝子治療を受けた患者の治療結果は改善され,潜在的に幹細胞移植の代替案となった.

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