Omenn's reticulosis associated with the nephrotic syndrome

M. Rybojad, S. Cambiaghi, I. Moraillon, M. D. Vignon-Pennamen, P. Morel, V. Baudoin, C. Loirat

Research output: Contribution to journalArticlepeer-review

Abstract

Omenn's reticulosis is an inherited severe combined immunodeficiency characterized be neonatal exfoliative erythroderma. A newborn baby who had minimal change nephrotic syndrome and Omenn's reticulosis is reported. Abnormalities in lymphocyte function could explain both the nephropathy and the cutaneous changes.

Original languageEnglish
Pages (from-to)124-127
Number of pages4
JournalBritish Journal of Dermatology
Volume135
Issue number1
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Dermatology

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