Abstract
Manifestations of immunodeficiency within the same family are presumed to be the same disease. We report a consanguineous extended family where four patients have immunodeficiency, three have X-linked agammaglobulinaemia and one has major histocompatibility complex class 2 deficiency. Within one family, two rare genetic diseases with similar clinical manifestations can occur.
| Original language | English |
|---|---|
| Pages (from-to) | 223-226 |
| Number of pages | 4 |
| Journal | International Journal of Immunogenetics |
| Volume | 36 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1 Aug 2009 |
ASJC Scopus subject areas
- Immunology
- Molecular Biology
- Genetics
- Genetics(clinical)
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