Literature DB >> 16630930

Primary immunodeficiency or not? Making the correct diagnosis.

Rebecca H Buckley1.   

Abstract

Making a correct diagnosis of a primary immunodeficiency disease is crucial for the selection of proper therapy. Although many cases go undiagnosed, there are also many instances of incorrect diagnosis that result in years of inappropriate treatment and failure to implement beneficial treatment. This article summarizes 2 actual cases in which incorrect diagnoses led to recommendations of unwarranted high-risk or costly treatments. Had the physicians chosen tests of immune function rather than relying on immunoglobulin levels or cell counts, they would have arrived at the true diagnoses.

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Year:  2006        PMID: 16630930     DOI: 10.1016/j.jaci.2006.01.008

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  11 in total

1.  Positive Family History, Infection, Low Absolute Lymphocyte Count (ALC), and Absent Thymic Shadow: Diagnostic Clues for All Molecular Forms of Severe Combined Immunodeficiency (SCID).

Authors:  Laurie M McWilliams; Mary Dell Railey; Rebecca H Buckley
Journal:  J Allergy Clin Immunol Pract       Date:  2015-03-29

2.  A Clinical Approach to a Child with Hypoalbuminemia and Lymphopenia.

Authors:  Ayse Sevgi Köstel-Bal; Suna Kaymak; Şule Haskoloğlu; Zarife Kuloğlu; Arzu Ensari; Figen Doğu; Aydan Kansu; Aydan İkincioğulları
Journal:  J Clin Immunol       Date:  2016-03-30       Impact factor: 8.317

Review 3.  Should newborns be screened for immunodeficiency?: lessons learned from infants with recurrent otitis media.

Authors:  Yesim Yilmaz-Demirdag
Journal:  Curr Allergy Asthma Rep       Date:  2011-12       Impact factor: 4.806

Review 4.  Common dermatologic manifestations of primary immune deficiencies.

Authors:  Manisha Relan; Heather K Lehman
Journal:  Curr Allergy Asthma Rep       Date:  2014-12       Impact factor: 4.919

Review 5.  Common variable immunodeficiency: etiological and treatment issues.

Authors:  Sean Deane; Carlo Selmi; Stanley M Naguwa; Suzanne S Teuber; M Eric Gershwin
Journal:  Int Arch Allergy Immunol       Date:  2009-07-01       Impact factor: 2.749

6.  Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a Coronin-1A mutation and a chromosome 16p11.2 deletion.

Authors:  Lawrence R Shiow; Kenneth Paris; Matthew C Akana; Jason G Cyster; Ricardo U Sorensen; Jennifer M Puck
Journal:  Clin Immunol       Date:  2008-12-20       Impact factor: 3.969

7.  Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings.

Authors:  Nicholas Brodszki; Göran Jönsson; Lillemor Skattum; Lennart Truedsson
Journal:  BMC Immunol       Date:  2014-08-14       Impact factor: 3.615

Review 8.  Patterns of Allergic Sensitization in High IgE Syndromes.

Authors:  Monica G Lawrence
Journal:  Curr Allergy Asthma Rep       Date:  2015-12       Impact factor: 4.919

Review 9.  Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice.

Authors:  Beatriz Tavares Costa-Carvalho; Anete Sevciovic Grumach; José Luis Franco; Francisco Javier Espinosa-Rosales; Lily E Leiva; Alejandra King; Oscar Porras; Liliana Bezrodnik; Mathias Oleastro; Ricardo U Sorensen; Antonio Condino-Neto
Journal:  J Clin Immunol       Date:  2013-11-16       Impact factor: 8.317

10.  Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?

Authors:  Lale Memmedova; Elif Azarsiz; Neslihan Edeer Karaca; Guzide Aksu; Necil Kutukculer
Journal:  Pediatr Rep       Date:  2013-09-17
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