SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik und Poliklinik für Rheumatologie im Asklepios Klinikum Bad Abbach

Description of facility

Director / Spokesperson
Prof. Dr. med. Martin Fleck
Information
Care facility for adults and children
Description
In Deutschland sind schätzungsweise eine Million Menschen von einer rheumatischen Erkrankung betroffen. Dabei gibt es „das Rheuma“ nicht: Vielmehr zählen mehr als 400 verschiedene Leiden zum rheumatischen Formenkreis. An der Klinik wird Ihren Schmerzen genau auf den Grund gegangen, um schnellstmöglich mit der passenden Therapie zu beginnen und Ihre Lebensqualität zu verbessern.
In der Klinik werden pro Jahr über 2.000 Patienten stationär aufgenommen und behandelt, mehr als 3.000 ambulant. Zusammen mit der Klinik und der Poliklinik für Innere Medizin I der Universität Regensburg bildet die Klinik und Poliklinik für Rheumatologie im Asklepios Klinikum Bad Abbach das Rheumazentrum Regensburg-Bad Abbach. Auf Basis von umfassenden Erfahrungswerten und eines Kompetenznetzes sind Sie an der Klinik in sehr guten Händen.
An der Klinik und Poliklinik für Rheumatologie im Asklepios Klinikum Bad Abbach werden folgende seltene Erkrankungen betreut: Systemische Sklerose, Polychondritis, Angeborene Immundefekte, Autoinflammatorische Syndrome.

Consultation hours

nach Vereinbarung.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy
  • Contact person for patients with an unclear diagnosis

Contact

Auskunft
09405 182219
09405 182910
Website http://www.asklepios.com/klinik/default.aspx?cid=681&pc=0402&did3=3982

Address

Kaiser-Karl-V.-Allee 3
93077 Bad Abbach

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Preview of the assigned diseases 4

Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib Hyperzincemia and hypercalprotectinemia Recurrent infection due to specific granule deficiency Pearson syndrome Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Immunodeficiency due to a classical component pathway complement deficiency Herpes simplex virus encephalitis Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency Nakajo-Nishimura syndrome Immunodeficiency due to MASP-2 deficiency Immunodeficiency due to a late component of complement deficiency Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency Epidermodysplasia verruciformis Muckle-Wells syndrome Chédiak-Higashi syndrome Constitutional neutropenia with extra-hematopoietic manifestations Immunodeficiency due to ficolin3 deficiency Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency Other immunodeficiency syndromes due to defects in innate immunity Granulomatous autoinflammatory syndrome X-linked severe congenital neutropenia X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency Hereditary periodic fever syndrome X-linked mendelian susceptibility to mycobacterial diseases Relapsing polychondritis Kostmann syndrome NLRP12-associated hereditary periodic fever syndrome Severe congenital neutropenia Pyogenic autoinflammatory syndrome Autoinflammatory syndrome with immune deficiency Blau syndrome PASH syndrome Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Mixed autoinflammatory and autoimmune syndrome Unclassified autoinflammatory syndrome Cohen syndrome Immunodeficiency with factor I anomaly Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency Rare systemic or rheumatological disease of childhood X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency Immunodeficiency with factor H anomaly Mendelian susceptibility to mycobacterial diseases Hypohidrotic ectodermal dysplasia with immunodeficiency Recurrent Neisseria infections due to factor D deficiency Familial Mediterranean fever Hyperimmunoglobulinemia D with periodic fever Lichtenstein syndrome Sterile multifocal osteomyelitis with periostitis and pustulosis Infantile onset panniculitis with uveitis and systemic granulomatosis Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Generalized pustular psoriasis Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency Autosomal dominant severe congenital neutropenia Idiopathic recurrent pericarditis Unexplained periodic fever syndrome WHIM syndrome MAGIC syndrome Idiopathic CD4 lymphocytopenia CINCA syndrome PFAPA syndrome Tumor necrosis factor receptor 1 associated periodic syndrome Erdheim-Chester disease Congenital neutropenia-myelofibrosis-nephromegaly syndrome Poikiloderma with neutropenia Cyclic neutropenia Rare systemic or rheumatologic disease Pyoderma gangrenosum Functional neutrophil defect T-cell immunodeficiency with epidermodysplasia verruciformis Griscelli syndrome type 2 Proteasome-associated autoinflammatory syndrome Hermansky-Pudlak syndrome due to AP-3 deficiency Neutropenia-monocytopenia-deafness syndrome Majeed syndrome Autoinflammatory syndrome Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency Properdin deficiency Primary immunodeficiency due to a defect in innate immunity Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency Constitutional neutropenia Leukocyte adhesion deficiency Schnitzler syndrome NLRP3-associated autoinflammatory disease Immunodeficiency due to a complement cascade protein anomaly Chronic granulomatous disease Chronic mucocutaneous candidiasis Monocytopenia with susceptibility to infections JMP syndrome SAPHO syndrome PAPA syndrome Barth syndrome Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency Periodic fever syndrome Sarcoidosis Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency Behçet disease Complement component 3 deficiency Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency Neutrophil immunodeficiency syndrome Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency Diffuse cutaneous systemic sclerosis CANDLE syndrome Genetic susceptibility to infections due to particular pathogens Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency Familial cold urticaria Shwachman-Diamond syndrome Bacterial susceptibility due to TLR signaling pathway deficiency Myeloperoxidase deficiency Papillon-Lefèvre syndrome Limited cutaneous systemic sclerosis CREST syndrome Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Limited systemic sclerosis Systemic sclerosis Susceptibility to viral and mycobacterial infections due to STAT1 deficiency Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency Primary immunodeficiency syndrome due to LAMTOR2 deficiency Leukocyte adhesion deficiency type III Leukocyte adhesion deficiency type II Leukocyte adhesion deficiency type I Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome DITRA Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
12.03321039676666448.928519341175075Klinik und Poliklinik für Rheumatologie im Asklepios Klinikum Bad Abbach
Last updated: 12.10.2022