| Literature DB >> 21748095 |
Ibtisam B Elnour1, Shakeel Ahmed, Kamal Halim, V Nirmala.
Abstract
Over the last 17 years different forms of severe combined immunodeficiency have been diagnosed at Sultan Qaboos University Hospital, Muscat. Omenn's syndrome is a rare autosomal recessive form of severe combined immunodeficiency. We report a 6 weeks old Omani infant who presented with the characteristic clinical and immunological phenotype of Omenn's syndrome. We take the opportunity to discuss and review the immunological aspect of this rare syndrome.Entities:
Keywords: Case report; Immunodeficiency, primary; Immunodeficiency, severe, combined; Oman; Omenn’s Syndrome
Year: 2007 PMID: 21748095 PMCID: PMC3074865
Source DB: PubMed Journal: Sultan Qaboos Univ Med J ISSN: 2075-051X