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Article

Omenn Syndrome Presenting with Striking Erythroderma and Extreme Lymphocytosis in a Newborn.

Pediatric dermatology - 1 Jan 2017

Zafar Rabia, Ver Heul Aaron, Beigelman Avraham, Bednarski Jeffrey J, Bayliss Susan J, Dehner Louis P, Rosman Ilana S, Coughlin Carrie C

Abstract excerpt

Omenn syndrome is an autosomal recessive form of "leaky" severe combined immune deficiency resulting in distinct phenotypic features. The patient described herein had an atypical presentation of Omenn syndrome, with conspicuous erythroderma and extreme lymphocytosis at birth, in contrast to the typical evolution of rash seen during the first few weeks of life. In addition, the skin findings were secondary to...

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Identifiers

PMID: 27862277
DOI: 10.1111/pde.13023

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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Omenn Syndrome Presenting with Striking Erythroderma and Extreme Lymphocytosis in a Newborn.PMID 27862277Read ↗

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