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Article

[MonoMAC syndrome].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 1 Aug 2014

Chen Zhao-Long, An Yun-Fei, Zhao Xiao-Dong

Abstract excerpt

MonoMAC syndrome is a newly discovered immune deficiency syndrome caused by GATA-2 mutation, which is an autosomal dominant genetic disease. MonoMAC syndrome has typical immune cell abnormalities, with severe infection and is prone to develop into a hematological disease. Therapeutics for this disease mainly relies on symptomatic treatment and hematopoietic stem cell transplantation. In this paper, the research...

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PMID: 25140787

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Rheumatologic manifestations of the "MonoMAC" syndrome. a systematic review.Semantic proximity Read ↗

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Haematopoietic and immune defects associated with GATA2 mutation.Semantic proximity Read ↗

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GATA2 deficiency and haematopoietic stem cell transplantation: challenges for the clinical practitionerSemantic proximity Read ↗

From clinical observations and molecular dissection to novel therapeutic strategies for primary immunodeficiency disorders.Semantic proximity Read ↗

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