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Article

Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.

European journal of pediatrics - 1 Aug 2011

Karaca Neslihan Edeer, Durandy Anne, Gulez Nesrin, Aksu Guzide, Kutukculer Necil

Abstract excerpt

UNLABELLED: Hyper-IgM syndromes are characterized by normal or elevated serum IgM levels with the absence or reduced levels of other immunoglobulins. There are some patients with defective class-switch recombination (CSR) who do not have CD40L, CD40, AID, and UNG defects. The aim of this study is...

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Source

Identifiers

PMID: 21274562
DOI: 10.1007/s00431-011-1400-2

Genes

UNG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21274562-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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