» Articles » PMID: 30923334

Regarding the Rights and Duties of Clinical Laboratory Geneticists in Genetic Healthcare Systems; Results of a Survey in over 50 Countries

Overview
Journal Eur J Hum Genet
Specialty Genetics
Date 2019 Mar 30
PMID 30923334
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Specialists of human genetic diagnostics can be divided into four groups: Medical Geneticists (MDG), Genetic Nurses and/or Counsellors (GN/GC), Clinical Laboratory Geneticists (CLG) and Laboratory Genetics Technicians (LGT). While the first two groups are in direct patient contact, the work of the latter two, of equal importance for patient care, are often hidden as they work behind the scenes. Herein the first study on the rights and duties of CLGs is presented. We present the results of a survey performed in 35 European and 18 non-European countries with 100 participating specialists. A national CLG title is available in 60% of European countries, and in 77% of the surveyed European countries a CLG can be the main responsible head of the laboratory performing human genetic tests. However, in only 20% of European countries is a lab-report valid with only a CLGs' signature - even though the report is almost always formulated by the CLG, and an interpretation of the obtained results in a clinical context by the CLG is expected in nearly 90% of European countries. Interestingly, CLGs see patients in 30% of European countries, and are also regularly involved in student education. Overall, the CLG profession includes numerous duties, which are quite similar in all regions of the world. Strikingly, the CLG's rights and responsibilities of leading a lab, or signing a report are regulated differently according to country specific regulations. Overall, the CLG is a well-recognized profession worldwide and often working within a multidisciplinary team of human genetic diagnostics professionals.

Citing Articles

Exploring current challenges in the technologist workforce of clinical genomics laboratories.

Akkari Y, Dobin S, Best R, Leung M Genet Med Open. 2024; 1(1):100806.

PMID: 39669260 PMC: 11613654. DOI: 10.1016/j.gimo.2023.100806.


.

Hollstein R, Ishorst N, Lischka A, Sindermann L, Behrens Y Med Genet. 2024; 35(4):339-350.

PMID: 38841540 PMC: 11006294. DOI: 10.1515/medgen-2023-2045.


.

Paneque M, Serra Juhe C, Melegh B, Carreira I, Moog U, Liehr T Med Genet. 2024; 34(1):81-83.

PMID: 38836018 PMC: 11006253. DOI: 10.1515/medgen-2022-2116.


.

Paneque M, Serra Juhe C, Melegh B, Carreira I, Moog U, Liehr T Med Genet. 2024; 34(2):189-191.

PMID: 38835907 PMC: 11006359. DOI: 10.1515/medgen-2022-2122.


Non-Invasive Prenatal Testing in Germany.

Liehr T, Harutyunyan T, Williams H, Weise A Diagnostics (Basel). 2022; 12(11).

PMID: 36428876 PMC: 9689121. DOI: 10.3390/diagnostics12112816.


References
1.
Liehr T, Carreira I, Aktas D, Bakker E, de Alba M, Coviello D . European registration process for Clinical Laboratory Geneticists in genetic healthcare. Eur J Hum Genet. 2017; 25(5):515-519. PMC: 5437904. DOI: 10.1038/ejhg.2017.25. View

2.
Lewis C, Kent A, Skirton H, Coviello D . EuroGentest patient information leaflets: a free resource available in over 20 languages. Eur J Hum Genet. 2009; 17(6):732. PMC: 2947104. DOI: 10.1038/ejhg.2009.20. View

3.
Wolff G . [Basic principles of genetic counseling]. Diskussionsforum Med Ethik. 1992; (9-10):LVI-LVIII. View

4.
Cassiman J . Research network: EuroGentest--a European Network of Excellence aimed at harmonizing genetic testing services. Eur J Hum Genet. 2005; 13(10):1103-5. DOI: 10.1038/sj.ejhg.5201484. View

5.
Paneque M, Serra-Juhe C, Pestoff R, Cordier C, Silva J, Moldovan R . Complementarity between medical geneticists and genetic counsellors: its added value in genetic services in Europe. Eur J Hum Genet. 2017; 25(8):918-923. PMC: 5567148. DOI: 10.1038/ejhg.2017.76. View