{"id":406,"date":"2022-02-08T13:42:10","date_gmt":"2022-02-08T12:42:10","guid":{"rendered":"https:\/\/ern-ithaca.eu\/?post_type=expert-centers&p=406"},"modified":"2022-03-08T15:06:26","modified_gmt":"2022-03-08T14:06:26","slug":"ern-ithaca-gottingen-center","status":"publish","type":"expert-centers","link":"https:\/\/ern-ithaca.eu\/it\/about-us\/expert-centers\/ern-ithaca-gottingen-center\/","title":{"rendered":"ERN-ITHACA \u2013 Centro di Gottinga"},"content":{"rendered":"
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Photo by umg\/rschmidt<\/figcaption><\/figure>\n\n\n\n

University Medical Center G\u00f6ttingen<\/strong>
Institute of Human Genetics
Heinrich-D\u00fcker-Weg 12
37073 G\u00d6TTINGEN
GERMANIA<\/p>\n\n\n\n

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Sito web<\/a><\/div>\n<\/div>\n\n\n\n
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Piombo<\/h2>\n\n\n\n
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Prof. Dr. med. Bernd Wollnik<\/strong><\/p>\n\n\n\n

Telephone: +49-551-39-67589<\/p>\n\n\n\n

Fax: +49-551-39-69303<\/p>\n\n\n\n

E-Mail: bernd.wollnik@med.uni-goettingen.de<\/a><\/p>\n<\/div>\n<\/div>\n\n\n\n

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Ambito di applicazione<\/h2>\n\n\n\n

The University Medical Center G\u00f6ttingen (UMG) has extensive experience in providing expert and patient-centered care for all congenital syndromes with malformations and\/or intellectual disability and offers patients high-end procedures and services related to prevention, acute care, ambulatory care, diagnostics, interventional therapeutic management, rehabilitation or social care.<\/p>\n\n\n\n

UMG’s Institute of Human Genetics is nationally and internationally recognized for its research activities to identify the genetic causes and molecular mechanisms underlying rare congenital disorders. Its key research focus lies on progeroid syndromes (e.g. Wiedemann-Rautenstrauch syndrome, neonatal progeria syndromes, Hallermann-Streiff syndrome), microcephalic syndromes (e.g. Bloom syndrome, Seckel syndrome), malformation syndromes (e.g. Kabuki syndrome, CHARGE syndrome) and skeletal disorders (e.g. osteogenesis imperfecta). Its researchers also work to explore the potential of genome editing approaches to develop new therapeutic strategies for rare congenital diseases. Cutting-edge resources and services in genomics, transcriptomics and epigenomics are provided by the Institute of Human Genetics and also by NIG (NGS Integrative Genomics core unit), UMG’s central research service facility affiliated with the Institute of Human Genetics.<\/p>\n\n\n\n

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Assistenza ai pazienti<\/h2>\n\n\n\n

<\/a>In addition to its comprehensive inpatient and outpatient health care services of a university hospital, the G\u00f6ttingen Centre can rely on its highly-specialized expertise and infrastructure to offer the best possible care to patients and their families within the scope of ERN-ITHACA:<\/p>\n\n\n\n