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.
Publication details
- DOI
- 10.18295/2075-0528.2654
- Journal
- Sultan Qaboos University Medical Journal, 7(2), 133-138
- Publisher
- Sultan Qaboos University
- Open access
- Gold open access
- License
- CC BY-ND 4.0
Cite this article
APA 7
Elnour, I. B., Ahmed, S., & Nirmala, K. (2025). Omenn’s Syndrome: A rare primary immunodeficiency disorder. Sultan Qaboos University Medical Journal, 7(2), 133-138. https://doi.org/10.18295/2075-0528.2654
MLA 9
Elnour, Ibtisam B., et al. "Omenn’s Syndrome: A rare primary immunodeficiency disorder." Sultan Qaboos University Medical Journal, vol. 7, no. 2, 2025, pp. 133-138. https://doi.org/10.18295/2075-0528.2654.
Chicago (author–date)
Elnour, Ibtisam B., Shakeel Ahmed, and Kamal Nirmala. 2025. "Omenn’s Syndrome: A rare primary immunodeficiency disorder." Sultan Qaboos University Medical Journal 7 (2): 133-138. https://doi.org/10.18295/2075-0528.2654.
Harvard
Elnour, I. B., Ahmed, S. and Nirmala, K. (2025) 'Omenn’s Syndrome: A rare primary immunodeficiency disorder', Sultan Qaboos University Medical Journal, 7(2), pp. 133-138. doi:10.18295/2075-0528.2654.
Vancouver
Elnour IB, Ahmed S, Nirmala K. Omenn’s Syndrome: A rare primary immunodeficiency disorder. Sultan Qaboos University Medical Journal. 2025;7(2):133-138. doi:10.18295/2075-0528.2654
IEEE
I. B. Elnour, S. Ahmed, and K. Nirmala, "Omenn’s Syndrome: A rare primary immunodeficiency disorder," Sultan Qaboos University Medical Journal, vol. 7, no. 2, pp. 133-138, 2025, doi: 10.18295/2075-0528.2654.