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Article

Langerhans cell histiocytosis, a new clinical phenotype of x-linked lymphoproliferative disease?

European journal of medical genetics - 1 Jan 2000

Zhang Xiaoying, Zhu Dexin, Lan Hekui, Yu Li, Peng Wei, Mei Yabo, Feng Zhichun

Abstract excerpt

Langerhans' cell histiocytosis (LCH) is a rare disease of unkown cause and is characterized by clonal proliferation of Langerhans cells. Here, we describe the case of a 22-month-old boy with LCH associated with X-linked lymphoproliferative disease (XLP). Sequence analysis of SH2D1A for mutations...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21094704
DOI: 10.1016/j.ejmg.2010.11.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21094704-2026-09-04.1. Manifest publication-graph-cohort-2026-09-04.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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