Primary immune deficiencies presenting in adults: seven years of experience from Iran.

Details

Request a copyRequest a copy
Serval ID
serval:BIB_CC72F86C0775
Type
Article: article from journal or magazin.
Collection
Publications
Institution
UNIL/CHUV
Title
Primary immune deficiencies presenting in adults: seven years of experience from Iran.
Journal
Journal of clinical immunology
Author(s)
Mansouri D., Adimi P., Mirsaedi M., Mansouri N., Tabarsi P., Amiri M., Jamaati H.R., Motavasseli M., Baghaii N., Cheraghvandi A., Rouhi R., Roozbahany N.A., Zahirifard S., Mohammadi F., Masjedi M.R., Velayati A.A., Casanova J.L., Speert D.P., Elwood R.K., Schellenberg R., Turvey S.E.
ISSN
0271-9142 (Print)
ISSN-L
0271-9142
Publication state
Published
Issued date
07/2005
Peer-reviewed
Oui
Volume
25
Number
4
Pages
385-391
Language
english
Notes
Publication types: Case Reports ; Journal Article
Publication Status: ppublish
Abstract
Primary immunodeficiencies (PIDs) are not solely diseases of childhood. We describe the clinical presentation and outcome for 55 adult patients with previously unrecognized PIDs. This series provides unique data regarding PIDs presenting in adulthood, and serves as a timely reminder that physicians must consider the diagnosis of PIDs in their adult patients. Using the experience gained from these patients, we outline key "warning signs" suggestive of an underlying PID. Only through increased physician awareness will patients with PIDs receive timely diagnosis and optimal management.
Keywords
Adolescent, Adult, Agammaglobulinemia/diagnosis, Agammaglobulinemia/genetics, Agammaglobulinemia/immunology, Aged, Ataxia Telangiectasia/diagnosis, Ataxia Telangiectasia/genetics, Ataxia Telangiectasia/immunology, Common Variable Immunodeficiency/diagnosis, Common Variable Immunodeficiency/genetics, Common Variable Immunodeficiency/immunology, Complement C1 Inactivator Proteins/deficiency, Complement C1 Inhibitor Protein, Diagnosis, Differential, Female, Genetic Diseases, X-Linked/diagnosis, Genetic Diseases, X-Linked/genetics, Genetic Diseases, X-Linked/immunology, Humans, Immunity, Cellular/genetics, Immunoglobulins/biosynthesis, Immunoglobulins/deficiency, Immunoglobulins/genetics, Iran, Job Syndrome/diagnosis, Job Syndrome/genetics, Job Syndrome/immunology, Leukocyte-Adhesion Deficiency Syndrome/diagnosis, Leukocyte-Adhesion Deficiency Syndrome/genetics, Leukocyte-Adhesion Deficiency Syndrome/immunology, Male, Middle Aged, Neutropenia/diagnosis, Neutropenia/genetics, Neutropenia/immunology, Retrospective Studies, Serpins/deficiency, Wiskott-Aldrich Syndrome/diagnosis, Wiskott-Aldrich Syndrome/genetics, Wiskott-Aldrich Syndrome/immunology
OAI-PMH
oai:serval.unil.ch:BIB_CC72F86C0775
DOI
10.1007/s10875-005-4124-0
Pubmed
16133995
Web of science
000231317100011
Create date
04/02/2021 19:03
Last modification date
20/07/2022 5:39
Usage data