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-...

Full description

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/
id UDEA2_f106273e790f3134629df9331feac38d
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/43126
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
title A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
spellingShingle A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
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
title_short A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
title_full A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
title_fullStr A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
title_full_unstemmed A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
title_sort A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
dc.creator.fl_str_mv 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
dc.contributor.author.none.fl_str_mv 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
dc.contributor.researchgroup.spa.fl_str_mv Inmunodeficiencias Primarias
dc.subject.decs.none.fl_str_mv 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
topic 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
dc.subject.meshuri.none.fl_str_mv 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
description 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.
publishDate 2013
dc.date.issued.none.fl_str_mv 2013
dc.date.accessioned.none.fl_str_mv 2024-11-04T01:02:12Z
dc.date.available.none.fl_str_mv 2024-11-04T01:02:12Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.redcol.spa.fl_str_mv https://purl.org/redcol/resource_type/ART
dc.type.coarversion.spa.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
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dc.identifier.citation.spa.fl_str_mv Bousfiha AA, Jeddane L, Ailal F, Al Herz W, Conley ME, Cunningham-Rundles C, Etzioni A, Fischer A, Franco JL, Geha RS, Hammarström L, Nonoyama S, Ochs HD, Roifman CM, Seger R, Tang ML, Puck JM, Chapel H, Notarangelo LD, Casanova JL. A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside. J Clin Immunol. 2013 Aug;33(6):1078-87. doi: 10.1007/s10875-013-9901-6.
dc.identifier.issn.none.fl_str_mv 0271-9142
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/43126
dc.identifier.doi.none.fl_str_mv 10.1007/s10875-013-9901-6
dc.identifier.eissn.none.fl_str_mv 1573-2592
identifier_str_mv Bousfiha AA, Jeddane L, Ailal F, Al Herz W, Conley ME, Cunningham-Rundles C, Etzioni A, Fischer A, Franco JL, Geha RS, Hammarström L, Nonoyama S, Ochs HD, Roifman CM, Seger R, Tang ML, Puck JM, Chapel H, Notarangelo LD, Casanova JL. A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside. J Clin Immunol. 2013 Aug;33(6):1078-87. doi: 10.1007/s10875-013-9901-6.
0271-9142
10.1007/s10875-013-9901-6
1573-2592
url https://hdl.handle.net/10495/43126
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv J. Clin. Immunol.
dc.relation.citationendpage.spa.fl_str_mv 1087
dc.relation.citationissue.spa.fl_str_mv 6
dc.relation.citationstartpage.spa.fl_str_mv 1078
dc.relation.citationvolume.spa.fl_str_mv 33
dc.relation.ispartofjournal.spa.fl_str_mv Journal of Clinical Immunology
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dc.format.extent.spa.fl_str_mv 16 páginas
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dc.publisher.spa.fl_str_mv Springer
dc.publisher.place.spa.fl_str_mv Ámsterdam, Países Bajos
institution Universidad de Antioquia
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spelling Franco Restrepo, José LuisBousfiha, Ahmed AzizJeddane, LeïlaAilal, FatimaAl Herz, WaleedConley, Mary EllenCunningham Rundles, CharlotteEtzioni, AmosFischer, AlainGeha, Raif S.Hammarström, LennartNonoyama, ShigeakiOchs, Hans D.Roifman, Chaim M.Seger, ReinhardTang, Mimi L. K.Puck, Jennifer M.Chapel, HelenNotarangelo, Luigi D.Casanova, Jean LaurentInmunodeficiencias Primarias2024-11-04T01:02:12Z2024-11-04T01:02:12Z2013Bousfiha AA, Jeddane L, Ailal F, Al Herz W, Conley ME, Cunningham-Rundles C, Etzioni A, Fischer A, Franco JL, Geha RS, Hammarström L, Nonoyama S, Ochs HD, Roifman CM, Seger R, Tang ML, Puck JM, Chapel H, Notarangelo LD, Casanova JL. A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside. J Clin Immunol. 2013 Aug;33(6):1078-87. doi: 10.1007/s10875-013-9901-6.0271-9142https://hdl.handle.net/10495/4312610.1007/s10875-013-9901-61573-2592ABSTRACT: 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.National Institutes of HealthCOL001242616 páginasapplication/pdfengSpringerÁmsterdam, Países Bajoshttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the BedsideArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAlgorithmsAlgoritmosDiagnosis, DifferentialDiagnóstico DiferencialDiagnostic Tests, RoutinePruebas Diagnósticas de RutinaGenotypeGenotipoImmunologic Deficiency SyndromesSíndromes de InmunodeficienciaImmunologic TestsPruebas InmunológicasPhenotypeFenotipoPractice Guidelines as TopicGuías de Práctica Clínica como Asuntohttps://id.nlm.nih.gov/mesh/D000465https://id.nlm.nih.gov/mesh/D003937https://id.nlm.nih.gov/mesh/D003955https://id.nlm.nih.gov/mesh/D005838https://id.nlm.nih.gov/mesh/D007153https://id.nlm.nih.gov/mesh/D007159https://id.nlm.nih.gov/mesh/D010641https://id.nlm.nih.gov/mesh/D017410J. Clin. 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