Omenn's syndrome. A rare primary immunodeficiency disorder
SQUMJ-Sultan Qaboos University Medical Journal. 2007; 7 (2): 63-68
em Inglês
| IMEMR
| ID: emr-85286
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
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Esplenomegalia
/
Síndrome
/
Hepatomegalia
/
Doenças Linfáticas
Tipo de estudo:
Relato de Casos
Limite:
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Sultan Qaboos Univ. Med. J.
Ano de publicação:
2007
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