A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
ABSTRACT: The number of genetically defined Primary Immunodeficiency Diseases (PID) has increased exponentially, especially in the past decade. The biennial classification published by the IUIS PID expert committee is therefore quickly expanding, providing valuable information regarding the disease-...
- Autores:
-
Franco Restrepo, José Luis
Bousfiha, Ahmed Aziz
Jeddane, Leïla
Ailal, Fatima
Al Herz, Waleed
Conley, Mary Ellen
Cunningham Rundles, Charlotte
Etzioni, Amos
Fischer, Alain
Geha, Raif S.
Hammarström, Lennart
Nonoyama, Shigeaki
Ochs, Hans D.
Roifman, Chaim M.
Seger, Reinhard
Tang, Mimi L. K.
Puck, Jennifer M.
Chapel, Helen
Notarangelo, Luigi D.
Casanova, Jean Laurent
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2013
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/43126
- Acceso en línea:
- https://hdl.handle.net/10495/43126
- Palabra clave:
- Algorithms
Algoritmos
Diagnosis, Differential
Diagnóstico Diferencial
Diagnostic Tests, Routine
Pruebas Diagnósticas de Rutina
Genotype
Genotipo
Immunologic Deficiency Syndromes
Síndromes de Inmunodeficiencia
Immunologic Tests
Pruebas Inmunológicas
Phenotype
Fenotipo
Practice Guidelines as Topic
Guías de Práctica Clínica como Asunto
https://id.nlm.nih.gov/mesh/D000465
https://id.nlm.nih.gov/mesh/D003937
https://id.nlm.nih.gov/mesh/D003955
https://id.nlm.nih.gov/mesh/D005838
https://id.nlm.nih.gov/mesh/D007153
https://id.nlm.nih.gov/mesh/D007159
https://id.nlm.nih.gov/mesh/D010641
https://id.nlm.nih.gov/mesh/D017410
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by/4.0/
| Summary: | ABSTRACT: The number of genetically defined Primary Immunodeficiency Diseases (PID) has increased exponentially, especially in the past decade. The biennial classification published by the IUIS PID expert committee is therefore quickly expanding, providing valuable information regarding the disease-causing genotypes, the immunological anomalies, and the associated clinical features of PIDs. These are grouped in eight, somewhat overlapping, categories of immune dysfunction. However, based on this immunological classification, the diagnosis of a specific PID from the clinician's observation of an individual clinical and/or immunological phenotype remains difficult, especially for non-PID specialists. The purpose of this work is to suggest a phenotypic classification that forms the basis for diagnostic trees, leading the physician to particular groups of PIDs, starting from clinical features and combining routine immunological investigations along the way. We present 8 colored diagnostic figures that correspond to the 8 PID groups in the IUIS Classification, including all the PIDs cited in the 2011 update of the IUIS classification and most of those reported since. |
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