Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children

Am J Med Genet A. 2021 Dec;185(12):3895-3896. doi: 10.1002/ajmg.a.62420. Epub 2021 Jul 12.

Authors

Lorenzo Calligaris¹, Luisa Cortellazzo Wiel², Emma Sartor², Irene Berti¹, Irene Bruno¹, Egidio Barbi^{1

2}, Andrea Magnolato¹

Affiliations

¹ Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
² Department of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.

PMID: 34250743
DOI: 10.1002/ajmg.a.62420

No abstract available

MeSH terms

Adolescent
Child
Child, Preschool
Female
Genetic Predisposition to Disease*
Humans
Infant
Male
Neurofibromatosis 1 / complications
Neurofibromatosis 1 / diagnosis*
Neurofibromatosis 1 / genetics
Neurofibromatosis 1 / pathology
Risk Factors
Xanthogranuloma, Juvenile / complications
Xanthogranuloma, Juvenile / diagnosis*
Xanthogranuloma, Juvenile / genetics
Xanthogranuloma, Juvenile / pathology