Omenn's reticulosis associated with the nephrotic syndrome

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

Omenn's reticulosis associated with the nephrotic syndrome

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

Fondazione IRCCS Ca' Granda- Ospedale Maggiore Policlinico

Research output: Contribution to journal › Article › peer-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 language	English
Pages (from-to)	124-127
Number of pages	4
Journal	British Journal of Dermatology
Volume	135
Issue number	1
Publication status	Published - 1996

ASJC Scopus subject areas

Dermatology

Cite this

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title = "Omenn's reticulosis associated with the nephrotic syndrome",

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.",

author = "M. Rybojad and S. Cambiaghi and I. Moraillon and Vignon-Pennamen, {M. D.} and P. Morel and V. Baudoin and C. Loirat",

year = "1996",

language = "English",

volume = "135",

pages = "124--127",

journal = "British Journal of Dermatology",

issn = "0007-0963",

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T1 - Omenn's reticulosis associated with the nephrotic syndrome

AU - Rybojad, M.

AU - Cambiaghi, S.

AU - Moraillon, I.

AU - Vignon-Pennamen, M. D.

AU - Morel, P.

AU - Baudoin, V.

AU - Loirat, C.

PY - 1996

Y1 - 1996

N2 - 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.

AB - 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.

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M3 - Article

C2 - 8776375

AN - SCOPUS:0029943233

VL - 135

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EP - 127

JO - British Journal of Dermatology

JF - British Journal of Dermatology

SN - 0007-0963

IS - 1

ER -

Omenn's reticulosis associated with the nephrotic syndrome

Abstract

ASJC Scopus subject areas

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