Imerslund-Gräsbeck Syndrome Caused by Compound Heterozygous Mutations in the AMN Gene: A Case Report
Cheng Chen1, Yijia Min2, Xiaoping Ye2
1Peking University First Hospital Ningxia Women and Children's Hospital (Ningxia Hui Autonomous Region Maternal and Child Health Hospital) Yinchuan Ningxia China.
Clinical Case Reports
|August 21, 2026
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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