Prenatal Fetal Neurocutaneous Melanosis: A Case Report and Literature Review
We reported a rare case of prenatal NCM, but no known pathogenic mutations, such as NRAS gene mutations, were found. This confirmed that there might be no definite pathogenic mutations in the NCM case, providing important data support for the prenatal identification and diagnosis of NCM. We reported a rare case of prenatal NCM, but no known pathogenic mutations, such as NARS gene mutations, were found. This confirmed that there might be no definite pathogenic mutations in the NCM case, providing important data support for the prenatal identification and diagnosis of NCM.
Authors
- Qiang Ma (ORCID: https://orcid.org/0009-0003-8752-5132)
- Xiaoying Zhang (ORCID: https://orcid.org/0000-0002-8130-1889)
- Y. Gu
- Yiwen He (ORCID: https://orcid.org/0000-0002-3841-4431)
- Xue Zhao (ORCID: https://orcid.org/0009-0003-4171-8967)
- Jing Wang
- Juan Song
- Li Lin
Institutions
- Peking University (CN)
- Peking University International Hospital (CN)
Publication Details
- Journal
- Molecular Genetics & Genomic Medicine
- Published
- 2025-12-31
- DOI
- https://doi.org/10.1002/mgg3.70174
- Primary Topic
- Cutaneous Melanoma Detection and Management
- Type
- article
- Field-Weighted Citation Impact
- 0.00