Polyposis, MUTYH-associated (MAP, FAP2)
Required sample material
Molecular genetic analysis:
3-7 ml EDTA blood or extracted DNA
Sample dispatch
EDTA blood samples and extracted DNA for molecular genetic analyses can usually be sent unrefrigerated by normal post, as the DNA extracted from the leucocytes is very stable. Intermediate storage (max. 7 days) should take place in the refrigerator.
Please send the samples to the following address:
Heidelberg University Hospital
Institute of Human Genetics
Laboratory for Molecular Genetic Diagnostics
Im Neuenheimer Feld 366
69120 Heidelberg
Sample labelling
Please label each sample container clearly with the surname, first name and date of birth of the patient and use our request forms.
The request forms are structured in such a way that we have all the necessary information about the patient and the patient consent form (where required) for the examination order.
Please complete the request forms carefully to avoid unnecessary enquiries. Please understand that we cannot accept unlabelled sample containers.
Please bear in mind that we can only carry out genetic analyses if we have the patient's written consent!
Request form for molecular genetics (German) (English)
Further information
OMIM:608456
Test method:
Complete variant screening in the MUTYH gene (16 exons) using Sanger sequencing or detection of (probable) pathogenic variants known in the family.
Note:
An interdisciplinary consultation (gastroenterology, human genetics, psycho-oncology if necessary) must have taken place before predictive testing.
Please also note that we must have received the patient's declaration of consent for molecular MUTYH diagnostics before starting predictive testing. The declaration of consent is part of our request form.
Processing time: 1-4 weeks on average
In rare cases, the processing time may be delayed by approx. 2 weeks.
Contact person
Dr. rer. nat. Christian Sutter
Focus
Hereditary tumor diseases, Head of Sanger sequencing core