Recurrent and unusual manifestations of tuberculosis in a boy with interleukin 12 receptor defect
| dc.contributor.author | Senanayake, M. P. | |
| dc.contributor.author | Doffinger, R. | |
| dc.contributor.author | D S Kumararatne, D. S. | |
| dc.date.accessioned | 2021-08-18T05:19:04Z | |
| dc.date.available | 2021-08-18T05:19:04Z | |
| dc.date.issued | 2009 | |
| dc.description.abstract | A genetically determined susceptibility to mycobacterial disease due to a specific immunological deficiency has been described. Although known as Mendelian susceptibility to mycobacterial disease (MSMD) this entity has both clinical and genetic heterogeneity. We describe a Sri Lankan boy with recurrent and rare manifestations of mycobacterial disease in whom a complete interleukin 12 receptor defect was identified. | en_US |
| dc.identifier.citation | Senanayake, M. P., Doffinger, R., & Kumararatne, D. S. (2012). Recurrent and unusual manifestations of tuberculosis in a boy with interleukin 12 receptor defect. | en_US |
| dc.identifier.uri | http://archive.cmb.ac.lk/handle/70130/5764 | |
| dc.language.iso | en | en_US |
| dc.publisher | Sri Lanka Medical Association | en_US |
| dc.subject | tuberculosis | en_US |
| dc.subject | interleukin 12 | en_US |
| dc.title | Recurrent and unusual manifestations of tuberculosis in a boy with interleukin 12 receptor defect | en_US |
| dc.type | Article | en_US |