Molekulare Früherkennung in der Endokrinologie - auf dem Weg zur differenzierten Behandlung komplexer Hormon- und Stoffwechselstörungen [Molecular tests for (early) recognition of endocrine disorders - towards a sophisticated management of complex endocrine and metabolic diseases]

Details

Serval ID
serval:BIB_6648CF11C7C7
Type
Article: article from journal or magazin.
Collection
Publications
Title
Molekulare Früherkennung in der Endokrinologie - auf dem Weg zur differenzierten Behandlung komplexer Hormon- und Stoffwechselstörungen [Molecular tests for (early) recognition of endocrine disorders - towards a sophisticated management of complex endocrine and metabolic diseases]
Journal
Therapeutische Umschau. Revue therapeutique
Author(s)
Kopp P.
ISSN
0040-5930 (Print)
ISSN-L
0040-5930
Publication state
Published
Issued date
07/2010
Peer-reviewed
Oui
Volume
67
Number
7
Pages
367-373
Language
german
Notes
Publication types: English Abstract ; Journal Article ; Review
Publication Status: ppublish
Abstract
Genetic testing has a growing impact on clinical medicine in endocrinology. In many disorders, genetic tests permit establishing a diagnosis at the molecular level. Genetic testing has clinical relevance for early carrier detection that may result in early and targeted interventions, and it is important for genetic counseling. Moreover, a detailed understanding of the molecular pathogenesis of endocrine neoplasms is key for the development of novel, more specific therapies. The practitioner should be familiar with key principles and indications for genetic testing. However, it is of importance to recognize potential limitations of genetic analyses, and to inform patients and their relatives accordingly. This review provides a short overview about genetic analyses in the field of endocrinology that are relevant for the practicing physician.
Keywords
Early Diagnosis, Endocrine System Diseases/diagnosis, Endocrine System Diseases/genetics, Genetic Markers/genetics, Genetic Predisposition to Disease/genetics, Genetic Testing/methods, Humans, Metabolic Diseases/diagnosis, Metabolic Diseases/genetics, Molecular Probe Techniques, Polymorphism, Single Nucleotide/genetics
Pubmed
Create date
28/12/2020 16:01
Last modification date
29/12/2020 6:26
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