Literature DB >> 22129053

Primary immune deficiency disorders in the South Pacific: the clinical utility of a customized genetic testing program in New Zealand.

Rohan Ameratunga1, See-Tarn Woon, Maia Brewerton, Wikke Koopmans, Anthony Jordan, Shannon Brothers, Ranjeeta Singh.   

Abstract

Primary immune deficiency disorders (PIDs) are a group of diseases associated with a genetic susceptibility to recurrent infections, malignancy, autoimmunity, and allergy. The molecular basis of many of these disorders has been identified in the last two decades. Most are inherited as single gene defects. As discussed in this paper, identifying the underlying genetic defect plays a critical role in many areas-including patient management, diagnosis, identifying atypical presentations, family studies, providing prognostic information, prenatal diagnosis, and defining new diseases. New Zealand is a geographically isolated, developed country in the South Pacific. We have introduced a dedicated customized genetic testing service for PID patients in New Zealand. This accredited diagnostic program offers rapid turnaround times for genetic tests and minimizes the risk of laboratory errors. Here we review the clinical indications for genetic testing for PIDs based on cases referred to the molecular immunology diagnostic service at Auckland City Hospital.
© 2011 New York Academy of Sciences.

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Year:  2011        PMID: 22129053     DOI: 10.1111/j.1749-6632.2011.06238.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  13 in total

Review 1.  Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing.

Authors:  Rohan Ameratunga; Klaus Lehnert; See-Tarn Woon; David Gillis; Vanessa L Bryant; Charlotte A Slade; Richard Steele
Journal:  Clin Rev Allergy Immunol       Date:  2018-04       Impact factor: 8.667

Review 2.  New diagnostic criteria for common variable immune deficiency (CVID), which may assist with decisions to treat with intravenous or subcutaneous immunoglobulin.

Authors:  R Ameratunga; S-T Woon; D Gillis; W Koopmans; R Steele
Journal:  Clin Exp Immunol       Date:  2013-11       Impact factor: 4.330

3.  Droplet digital PCR for identifying copy number variations in patients with primary immunodeficiency disorders.

Authors:  See-Tarn Woon; Julia Mayes; Alexander Quach; Hilary Longhurst; Antonio Ferrante; Rohan Ameratunga
Journal:  Clin Exp Immunol       Date:  2022-05-12       Impact factor: 4.330

4.  Droplet digital PCR for identifying copy number variations in patients with primary immunodeficiency disorders.

Authors:  See-Tarn Woon; Julia Mayes; Alexander Quach; Hilary Longhurst; Antonio Ferrante; Rohan Ameratunga
Journal:  Clin Exp Immunol       Date:  2021-12-21       Impact factor: 5.732

5.  Hereditary Angioedema as a Metabolic Liver Disorder: Novel Therapeutic Options and Prospects for Cure.

Authors:  Rohan Ameratunga; Adam Bartlett; John McCall; Richard Steele; See-Tarn Woon; Constance H Katelaris
Journal:  Front Immunol       Date:  2016-11-30       Impact factor: 7.561

6.  Comprehensive genetic testing for primary immunodeficiency disorders in a tertiary hospital: 10-year experience in Auckland, New Zealand.

Authors:  See-Tarn Woon; Rohan Ameratunga
Journal:  Allergy Asthma Clin Immunol       Date:  2016-12-07       Impact factor: 3.406

7.  Clinical Implications of Digenic Inheritance and Epistasis in Primary Immunodeficiency Disorders.

Authors:  Rohan Ameratunga; See-Tarn Woon; Vanessa L Bryant; Richard Steele; Charlotte Slade; Euphemia Yee Leung; Klaus Lehnert
Journal:  Front Immunol       Date:  2018-01-26       Impact factor: 7.561

8.  X-linked agammaglobulinemia presenting with secondary hemophagocytic syndrome: a case report.

Authors:  Can Ozturk; Sumer Sutcuoglu; Berna Atabay; Afig Berdeli
Journal:  Case Rep Med       Date:  2013-01-21

Review 9.  Comparison of diagnostic criteria for common variable immunodeficiency disorder.

Authors:  Rohan Ameratunga; Maia Brewerton; Charlotte Slade; Anthony Jordan; David Gillis; Richard Steele; Wikke Koopmans; See-Tarn Woon
Journal:  Front Immunol       Date:  2014-09-15       Impact factor: 7.561

10.  Epistatic interactions between mutations of TACI (TNFRSF13B) and TCF3 result in a severe primary immunodeficiency disorder and systemic lupus erythematosus.

Authors:  Rohan Ameratunga; Wikke Koopmans; See-Tarn Woon; Euphemia Leung; Klaus Lehnert; Charlotte A Slade; Jessica C Tempany; Anselm Enders; Richard Steele; Peter Browett; Philip D Hodgkin; Vanessa L Bryant
Journal:  Clin Transl Immunology       Date:  2017-10-20
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