Molecular analysis of T<sup>-</sup>B<sup>-</sup>NK<sup>+ </sup>severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia

Molecular analysis of T<sup>-</sup>B<sup>-</sup>NK<sup>+ </sup>severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia

<p>Abstract</p> <p>Background</p> <p>Children with Severe Combined Immunodeficiency (SCID) lack autologous T lymphocytes and present with multiple infections early in infancy. Omenn syndrome is characterized by the sole emergence of oligoclonal auto-reactive T lymphocyt...

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Bibliographic Details
Main Authors: Al-Kayal Fadi, Al-Saud Bandar, Al-Dhekri Hasan, Arnaout Rand, Al-Muhsen Saleh, Al-Ghonaium Abdulaziz, Alsmadi Osama, Al-Saud Haya, Al-Mousa Hamoud
Format: Article
Language:English
Published: BMC 2009-11-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/10/116

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http://www.biomedcentral.com/1471-2350/10/116

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