Disseminated BCG disease revealing a partial deficiency in receptor 1 interferon gamma
We report on a case of disseminated BCGitis with an unusual presentation in a 4-month-old infant revealing a syndrome of Mendelian susceptibility to mycobacteria due to a partial dominant mutation of the interferon gamma receptor 1 gene.
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Veröffentlicht in: | Archives de pédiatrie : organe officiel de la Société française de pédiatrie 2015-09, Vol.22 (9), p.971 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | fre |
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Zusammenfassung: | We report on a case of disseminated BCGitis with an unusual presentation in a 4-month-old infant revealing a syndrome of Mendelian susceptibility to mycobacteria due to a partial dominant mutation of the interferon gamma receptor 1 gene. |
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ISSN: | 1769-664X |
DOI: | 10.1016/j.arcped.2015.06.007 |