NF1 with 47,XYY mosaicism diagnosed by mandibular neurofibromas
Abstract Neurofibromatosis type 1 (NF1) is an autosomal dominant nevus disease characterized by multiple manifestations, primarily café-au-lait macules and neurofibromas. Here, we present the case of an NF1 patient with 47,XYY mosaicism whose diagnosis was prompted by café-au-lait macules on the ski...
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Main Authors: | Erina Tonouchi, Kei-ichi Morita, Yosuke Harazono, Kyoko Hoshino, Tetsuya Yoda |
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Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2024-05-01
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Series: | Human Genome Variation |
Online Access: | https://doi.org/10.1038/s41439-024-00279-8 |
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