These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Omenn's reticulosis associated with the nephrotic syndrome. Author: Rybojad M, Cambiaghi S, Moraillon I, Vignon-Pennmen MD, Morel P, Baudoin V, Loirat C. Journal: Br J Dermatol; 1996 Jul; 135(1):124-7. PubMed ID: 8776375. Abstract: Omenn's reticulosis is an inherited severe combined immunodeficiency characterized by 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.[Abstract] [Full Text] [Related] [New Search]