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08:00
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Introduction |
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08:15
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What is well accepted in molecular genetic diagnostics in KDIGO and elsewhere.
Jaro Nagel, Weißwasser/Greifswald
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08:45
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Perspectives of molecular genetic diagnostics with 3rd generation sequencing.
Sebastian Ganschow, Berlin
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09:15
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Diversity of HLA characteristics - chimeras due to immunological necessity versus obstacles to transplant retention.
Gerald Schlaf, Halle/Saale
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09:45
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Coffee break |
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10:00
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Prospects for gene therapy.
Andrea Zobel, Berlin
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10:30
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Prospects for Alport syndrome genetic therapy.
Oliver Groß, Göttingen
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11:00
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AI application in the diagnosis of rare diseases.
Annette D. Wagner, Hannover
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11:30
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GestaltMatcher - AI-supported prima vista diagnosis.
Peter Krawitz, Bonn
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Case report: HNF1B mutation.
Mato Nagel, Weißwasser
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Case report: Loeys-Dietz syndrome.
Hansjörg Rothe, Weißwasser/Leipzig
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12:30
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Lunch break |
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13:30
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Pathobiochemistry and molecular genetics of complement disorders.
Peter Zipfel, Jena
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14:15
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Complement-targeting therapy options. Status and perspectives.
Alexander Paliege, Dresden
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Case report: TMA suspicion resolved.
Clemens Krull, Berlin
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15:15
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Coffee break |
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15:45
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Autoinflammatory diseases: Pathogenesis and case presentations.
Christian Stefan Haas, Rostock
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Case report: persistant urinary tract infections with CRP elevation.
Mato Nagel, Weißwasser
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16:30
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Genetically supported therapy of lipid metabolism disorders, the broader perspective.
Winfried März, Augsburg
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Phenotypes of CREB3L3 mutations.
Mato Nagel, Weißwasser
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16:30
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Innovative therapies for bone metabolism. Relevance for renal osteopathy?
Mato Nagel, Weißwasser
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Severe osteoporosis with renotubular dysfunction.
Mato Nagel, Weißwasser
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Rare case of vitamin D deficiency?
Susanne und Michel Morlot, Hannover
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17:45
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Summary |
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18:00
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Farewell |
You can find out more about these topics in our teaser.
The program may by subject to change without notice.