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...
Saved in:
Main Authors: | , , , , |
---|---|
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 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|