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Article

Juvenile xanthogranuloma in Noonan syndrome.

American journal of medical genetics. Part A - 1 Oct 2021

Ali Marwan M, Gilliam Amy E, Ruben Beth S, Tidyman William E, Rauen Katherine A

Abstract excerpt

Noonan syndrome (NS) is one of the common RASopathies. While the clinical phenotype in NS is variable, it is typically characterized by distinctive craniofacial features, cardiac defects, reduced growth, bleeding disorders, learning issues, and an increased risk of cancer. Several different genes cause NS, all of which are involved in the Ras/mitogen-activated protein kinase (Ras/MAPK) pathway. Juvenile...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 34032360
DOI: 10.1002/ajmg.a.62353
PMCID: PMC8446294

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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