Omenn's syndrome. A rare primary immunodeficiency disorder
SQUMJ-Sultan Qaboos University Medical Journal. 2007; 7 (2): 63-68
Dans Anglais
| 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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Indice:
Méditerranée orientale
Sujet Principal:
Splénomégalie
/
Syndrome
/
Hépatomégalie
/
Maladies lymphatiques
Type d'étude:
Enquête cas-témoins / Études cas/témoins
Limites du sujet:
Humains
/
Mâle
langue:
Anglais
Texte intégral:
Sultan Qaboos Univ. Med. J.
Année:
2007
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