File:PMC3078321 431 2011 1452 Fig2 HTML.png

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Summary

Description
English⧼Colon⧽ A newborn infant with Omenn’s syndrome due to a mutation in the RAG 1 gene. Note the confluent erythematous exfoliating, thickened rash with a “leathery” consistency and loss of hair and eyebrows (courtesy of The Paediatric Immunology Unit, Great North Children’s Hospital, Newcastle upon Tyne)
Date
Source https://openi.nlm.nih.gov/detailedresult?img=PMC3078321_431_2011_1452_Fig2_HTML&query=omenn%20syndrome&it=xg&req=4&npos=2
Author van der Burg M, Gennery AR

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English⧼Colon⧽ This file is licensed CC BY-NC 4.0

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current20:36, 6 May 2022Thumbnail for version as of 20:36, 6 May 2022512 × 712 (804 KB)Ozzie10aaaaUploaded a work by van der Burg M, Gennery AR from https://openi.nlm.nih.gov/detailedresult?img=PMC3078321_431_2011_1452_Fig2_HTML&query=omenn%20syndrome&it=xg&req=4&npos=2 with UploadWizard

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