Molekuláris genetikai vizsgálatok primer immundefektusokban

Author:

Erdős Melinda12

Affiliation:

1. Infektológiai és Gyermekimmunológiai Tanszék, Debreceni Egyetem, Általános Orvostudományi Kar Debrecen

2. St. Giles Laboratory of Human Genetics of Infectious Diseases, The Rockefeller University 1230 York Avenue, Box 163, New York, NY 10065, USA

Abstract

Abstract: Next generation sequencing methods represent the latest era of molecular genetic diagnostics. After a general introduction on primary immunodeficiencies, the author summarizes the importance of molecular genetic studies, especially next generation sequencing in the diagnosis of primary immunodeficiencies. Another purpose of the manuscript is to give a brief summary on the methodological basis of next generation sequencing. The author analyzes the advantages and disadvantages of primary immunodeficiency gene-panel sequencing and whole-exome and whole-genome sequencing. Primary immunodeficiency genes and diseases recognized by next generation sequencing is also summarized. Finally, the author emphasizes the indispensability of gene level diagnostics in primary immunodeficiencies and presents the results achieved in this field in Hungary. Orv Hetil. 2018; 159(49): 2095–2112.

Publisher

Akademiai Kiado Zrt.

Subject

General Medicine

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