Literature DB >> 14708957

Syndromic immunodeficiencies: genetic syndromes associated with immune abnormalities.

Jeffrey E Ming1, E Richard Stiehm, John M Graham.   

Abstract

In syndromic immunodeficiencies, clinical features not directly associated with the immune defect are prominent. Patients may present with either infectious complications or extra-immune medical issues. In addition to the immunologic abnormality, a wide range of organ systems may be affected. Patients may present with disturbances in skeletal, neurologic, dermatologic, or gastrointestinal function or development. These conditions can be caused by developmental abnormalities, chromosomal aberrations, metabolic disorders, or teratogens. For a number of these conditions, recent advances have resulted in an enhanced understanding of their genetic basis. The finding of immune deficits in a number of defined syndromes with congenital anomalies suggests that an underlying genetic syndrome should be considered in those patients in whom a significant non-immune feature is present.

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Year:  2003        PMID: 14708957     DOI: 10.1080/714037692

Source DB:  PubMed          Journal:  Crit Rev Clin Lab Sci        ISSN: 1040-8363            Impact factor:   6.250


  7 in total

Review 1.  Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update.

Authors:  E de Vries
Journal:  Clin Exp Immunol       Date:  2012-01       Impact factor: 4.330

2.  Membranous nephropathy in Schimke immuno-osseous dysplasia.

Authors:  Nihal Ozdemir; Harika Alpay; Abdullah Bereket; Gamze Bereket; Neşe Biyikli; Metin Aydoğan; Fulya Cakalağoğlu; Işin Kiliçaslan; Ihsan Akpinar
Journal:  Pediatr Nephrol       Date:  2006-03-29       Impact factor: 3.714

3.  Primary immunodeficiency associated with chromosomal aberration - an ESID survey.

Authors:  Ellen Schatorjé; Michiel van der Flier; Mikko Seppänen; Michael Browning; Megan Morsheimer; Stefanie Henriet; João Farela Neves; Donald Cuong Vinh; Laia Alsina; Anete Grumach; Pere Soler-Palacin; Thomas Boyce; Fatih Celmeli; Ekaterini Goudouris; Grant Hayman; Richard Herriot; Elisabeth Förster-Waldl; Markus Seidel; Annet Simons; Esther de Vries
Journal:  Orphanet J Rare Dis       Date:  2016-08-02       Impact factor: 4.123

4.  Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes.

Authors:  Delfien J Bogaert; Melissa Dullaers; Hye Sun Kuehn; Bart P Leroy; Julie E Niemela; Hans De Wilde; Sarah De Schryver; Marieke De Bruyne; Frauke Coppieters; Bart N Lambrecht; Frans De Baets; Sergio D Rosenzweig; Elfride De Baere; Filomeen Haerynck
Journal:  Sci Rep       Date:  2017-06-16       Impact factor: 4.379

5.  Infection risk among adults with down syndrome: a two group series of 101 patients in a tertiary center.

Authors:  Aurélien Guffroy; Yannick Dieudonné; Beatrice Uring-Lambert; Joelle Goetz; Yves Alembik; Anne-Sophie Korganow
Journal:  Orphanet J Rare Dis       Date:  2019-01-11       Impact factor: 4.123

6.  Non-hodgkin lymphoma in a child with schimke immuno-osseous dysplasia.

Authors:  Mitra Basiratnia; Alireza Baradaran-Heravi; Majid Yavarian; Bita Geramizadeh; Mehran Karimi
Journal:  Iran J Med Sci       Date:  2011-09

7.  A novel immunodeficiency syndrome associated with partial trisomy 19p13.

Authors:  Markus G Seidel; Celia Duerr; Stavroula Woutsas; Anette Schwerin-Nagel; Kambis Sadeghi; Jürgen Neesen; Sabine Uhrig; Elisangela Santos-Valente; Winfried F Pickl; Wolfgang Schwinger; Christian Urban; Kaan Boztug; Elisabeth Förster-Waldl
Journal:  J Med Genet       Date:  2014-01-15       Impact factor: 6.318

  7 in total

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