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 |
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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