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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Bibliographic Details
Main Authors: Erina Tonouchi, Kei-ichi Morita, Yosuke Harazono, Kyoko Hoshino, Tetsuya Yoda
Format: Article
Language:English
Published: Nature Publishing Group 2024-05-01
Series:Human Genome Variation
Online Access:https://doi.org/10.1038/s41439-024-00279-8
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