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◆ Clinical case reports2026-08-01

Imerslund-Gräsbeck Syndrome Caused by Compound Heterozygous Mutations in the AMN Gene: A Case Report.

Cheng Chen, Yijia Min, Xiaoping Ye, Yu Ma, Huiqing Ge, Jingying Chou, Xiaoling Yang, Yingying Cui, Xiaochun Zhang

原始摘要(英文原文)· Original abstract
The 7-year-old girl had recurrent anemia for 6 years, showing large cell anemia. The parent-derived AMN double heterozygous mutation was detected to confirm the diagnosis of IGS. The hemogram was normal after intramuscular injection of vitamin B12, and there were no other complications.
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Imerslund-Gräsbeck Syndrome Caused by Compound Heterozygous Mutations in the AMN Gene: A Case Report. — 科研速览 Science Skim