Fumarate Hydratase–Deficient Leiomyoma with Double Mutation Sites in the FH Gene: A Rare Case Report and Literature Review
We report a rare case of FH-deficient uterine leiomyoma with double mutation sites in the FH gene. Pathological examination and genetic testing are crucial for a definitive diagnosis.
Authors
- Wei Guo (ORCID: https://orcid.org/0000-0003-3482-5118)
- Dongdong Zhang (ORCID: https://orcid.org/0000-0001-7611-3114)
- Xing Gong (ORCID: https://orcid.org/0009-0005-7358-905X)
- Jie Chen (ORCID: https://orcid.org/0009-0003-2727-0289)
Institutions
- Hubei University of Medicine (CN)
Publication Details
- Journal
- International Journal of Women s Health
- Published
- 2024-12-01
- DOI
- https://doi.org/10.2147/ijwh.s444069
- Primary Topic
- Urologic and reproductive health conditions
- Type
- article
- Field-Weighted Citation Impact
- 0.00