الملخص
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.
بيانات النشر
- المعرّف الرقمي
- 10.18295/2075-0528.2654
- المجلة
- مجلة جامعة السلطان قابوس الطبية, 7(2), 133-138
- الناشر
- جامعة السلطان قابوس
- وصول مفتوح
- وصول مفتوح ذهبي
- الترخيص
- CC BY-ND 4.0
اقتبس هذه المقالة
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.
شيكاغو (المؤلف–التاريخ)
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.
هارفارد
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.
فانكوفر
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.