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Article

Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: a case of Omenn syndrome.

European journal of dermatology : EJD - 1 Jun 2017

Cuperus Edwin, Montfrans Joris M VAN, Gijn Mariëlle E VAN, Bastiaens Maarten T, Willigen Mirjam Ma DE, Leguit Roos J, Brijnzeel-Koomen Carla Afm, RusseL Ingrid Mb, Pasmans Suzanne Gma

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Identifiers

PMID: 28414192
DOI: 10.1684/ejd.2017.2992

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Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: a case of Omenn syndrome.PMID 28414192Read ↗

Diagnosing Omenn syndrome.Semantic proximity Read ↗

[Immunodeficiencies: an overview and various diagnostic difficulties].Semantic proximity Read ↗

[Clinical phenotype and gene diagnostic analysis of Omenn syndrome].Semantic proximity Read ↗

Omenn Syndrome Presenting with Striking Erythroderma and Extreme Lymphocytosis in a Newborn.Semantic proximity Read ↗

Omenn syndrome with mutation in RAG1 gene.Semantic proximity Read ↗

A neonate diagnosed with Noonan syndrome with myeloproliferative change.Semantic proximity Read ↗

Omenn syndrome--review of several phenotypes of Omenn syndrome and RAG1/RAG2 mutations in Japan.Semantic proximity Read ↗

Mutation c.256_257delAA in RAG1 Gene in Polish Children with Severe Combined Immunodeficiency: Diversity of Clinical Manifestations.Semantic proximity Read ↗

Omenn syndrome in an infant with IL7RA gene mutation.Semantic proximity Read ↗

Pneumocystosis revealing immunodeficiency secondary to TERC mutation.Semantic proximity Read ↗

'Novel' immunodeficiency syndrome may be a previously described entity.Semantic proximity Read ↗

When Rothmund-Thomson syndrome is not: two new cases of Clericuzio-type poikiloderma with neutropenia.Semantic proximity Read ↗

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