Omenn syndrome: the first case in qatar

摘要

Abstract Omenn syndrome is a rare form of severe combined immune deficiency (SCID) with distinctive clinical and immunologic features(1). It was first described by Omenn in 1965 under the title of: Familial Reticuloen-Dotheliosis with Eosinophilia(2),. Since then, over 45 cases has been described(1). In this paper; we are reporting the first case of Omenn's syndrome in Qatar community.