| Literature DB >> 1517466 |
S A Misbah1, G P Spickett, A Zeman, M M Esiri, T B Wallington, J B Kurtz, H M Chapel.
Abstract
A 24 year old man presented with an unusual primary combined immune deficiency syndrome characterised by a profound lymphopenia of CD4 cells, selective serum IgG2 subclass deficiency, poor polysaccharide antibody responses, disseminated warts, recurrent sinopulmonary infection and bronchiectasis. The developed progressive multifocal leucoencephalopathy (PML) in association with sclerosing cholangitis. Progressive multifocal leucoencephalopathy (PML) usually occurs as an opportunistic infection in patients with secondary defects in cellular immunity.Entities:
Mesh:
Year: 1992 PMID: 1517466 PMCID: PMC495194 DOI: 10.1136/jcp.45.7.624
Source DB: PubMed Journal: J Clin Pathol ISSN: 0021-9746 Impact factor: 3.411