The Centre for Rare Syndromic Diseases, which is part of the Institute of Human Genetics (Director: Prof. Dr. med. Nataliya Di Donato), deals with the diagnosis of syndromic diseases. A syndrome is a non-random combination of individual symptoms. Syndromes can be hereditary or non-hereditary and can manifest themselves in both childhood and adulthood.
Competencies of the specialist center
- Genetic counseling
- Creation of a family tree
- Clinical-genetic examination
- Molecular genetic testing
- Molecular cytogenetic examinations
- Cytogenetic examinations
- Development of guidelines
- Evaluation of early detection measures
- Family examinations
- Teaching
- research
Contact details
Hannover Medical School
Center for Rare Diseases OE 5130
B-Centre for Rare Syndromal Diseases
Carl-Neuberg-Str. 1
30625 Hannover
You can find further information under the following links:
You can find more information under the following links:
- To the website "Portal for rare diseases and orphan drugs" Orphanet
- To the website "Care atlas for people with rare diseases" SE-Atlas
- To the website "Alliance of Chronic Rare Diseases" ACHSE e.V.
Please refer to the list below for an overview of ZSE specialist centers participating in registries:
Clinical trials with the participation of ZSE-B centers:
You can download the current publications of this ZSE-B center as PDF files under the following link: