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]

Détails

ID Serval
serval:BIB_6648CF11C7C7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
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]
Périodique
Therapeutische Umschau. Revue therapeutique
Auteur⸱e⸱s
Kopp P.
ISSN
0040-5930 (Print)
ISSN-L
0040-5930
Statut éditorial
Publié
Date de publication
07/2010
Peer-reviewed
Oui
Volume
67
Numéro
7
Pages
367-373
Langue
allemand
Notes
Publication types: English Abstract ; Journal Article ; Review
Publication Status: ppublish
Résumé
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.
Mots-clé
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
Création de la notice
28/12/2020 16:01
Dernière modification de la notice
29/12/2020 6:26
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