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Article

Atypical Omenn Syndrome Due to RAG2 Gene Mutation, a Case Report.

Iranian journal of immunology : IJI - 1 Dec 2019

Pourvali Ali, Arshi Saba, Nabavi Mohammad, Bemanian Mohammad Hasan, Shokri Sima, Shahrooei Mohammad, Rezaei Nima, Fallahpour Morteza

Abstract excerpt

Severe Combined Immunodeficiency (SCID), characterized by a profound decrease in both the number and function of T cells, is related to more than 20 different mutations. Recombination-activating gene (RAG) 1 and 2 seem to be two of the most common forms presenting with various manifestations, including typical SCID, Omenn syndrome (OS), atypical SCID (AS), or delayed onset combined immunodeficiency with...

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Identifiers

PMID: 31885011
DOI: 10.22034/IJI.2019.80285

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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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