SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik für Pädiatrie mit Schwerpunkt Pneumologie, Immunologie und Intensivmedizin an der Charité Berlin

Description of facility

Director / Spokesperson
Prof. Dr. med. Marcus A. Mall
Information
Care facility for adults and children
Description

Die Klinik für Pädiatrie mit Schwerpunkt Pneumologie und Immunologie betreut akut und chronisch kranke Patienten mit allergologischen, pneumologischen, immunologischen und rheumatologischen Erkrankungen von der Geburt bis zum 18. Lebensjahr. Weiterhin betreut sie auch Patienten aller Altersgruppen mit der angeborenen Erkrankung Mukoviszidose (Cystische Fibrose). Angeboten werden ambulante Sprechstunden und Schulungen für den Umgang mit chronischen Erkrankungen.

Die Klinik ist Teil des Otto Heubner Centrums für Kinder- und Jugendmedizin der Charité, Universitätsmedizin Berlin.

Consultation hours

Telefonische Erreichbarkeit: Mo – Do 7:30 – 16:00 Uhr sowie Fr 7:30 – 14:30 Uhr.

Care provisions

This facility offers the following
  • Social / legal advice
  • Genetic counselling
  • Clinical studies / research
  • Diagnostic
  • Therapy
  • Contact person for patients with an unclear diagnosis

Contact

Sekretariat
030 450566131
030 450566931
Website http://www.charite-ppi.de/

Address

Augustenburger Platz 1
13353 Berlin
Geländeadresse: Mittelallee 8

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch
France.png Französisch
Russian_Federation.png Russisch

Certificates 2

European Reference Network 2

Preview of the assigned diseases 7

Primary ciliary dyskinesia Juvenile dermatomyositis Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis Immunodeficiency due to CD25 deficiency Immunodeficiency due to a complement cascade protein anomaly Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency LIG4 syndrome Barth syndrome Primary ciliary dyskinesia-retinitis pigmentosa syndrome NLRP3-associated autoinflammatory disease JMP syndrome Secondary interstitial lung disease specific to childhood associated with a granulomatous disease Chronic pneumonitis of infancy Ataxia-telangiectasia-like disorder Primary immunodeficiency PAPA syndrome Exposure-related interstitial lung disease Sarcoidosis Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency Tuberculosis X-linked immunoneurologic disorder Secondary interstitial lung disease specific to childhood associated with a metabolic disease Yellow nail syndrome Pediatric Castleman disease Short-limb skeletal dysplasia with severe combined immunodeficiency Combined immunodeficiency due to IL21R deficiency Behçet disease Diffuse panbronchiolitis Complement component 3 deficiency Combined immunodeficiency due to DOCK8 deficiency Non-specific interstitial pneumonia Asbestos intoxication Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency Anti-neutrophil cytoplasmic antibody-associated vasculitis Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency Idiopathic pulmonary fibrosis Pediatric systemic lupus erythematosus X-linked lymphoproliferative disease CANDLE syndrome Immunoglobulin heavy chain deficiency Autoimmune lymphoproliferative syndrome Giant cell arteritis Genetic susceptibility to infections due to particular pathogens Bloom syndrome Mixed cryoglobulinemia type II Familial cold urticaria Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency Severe combined immunodeficiency due to LCK deficiency Mixed connective tissue disease Neutrophil immunodeficiency syndrome Mixed cryoglobulinemia type III Langerhans cell histiocytosis specific to childhood Osteopetrosis-hypogammaglobulinemia syndrome Lymphangioleiomyomatosis Vici syndrome Shwachman-Diamond syndrome Familial hemophagocytic lymphohistiocytosis Say-Barber-Miller syndrome Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency Bacterial susceptibility due to TLR signaling pathway deficiency Myeloperoxidase deficiency Hypocomplementemic urticarial vasculitis Papillon-Lefèvre syndrome Chronic beryllium disease Brain-lung-thyroid syndrome Interstitial lung disease specific to adulthood Susceptibility to viral and mycobacterial infections due to STAT1 deficiency Facial dysmorphism-immunodeficiency-livedo-short stature syndrome CREST syndrome Hajdu-Cheney syndrome T-cell immunodeficiency with thymic aplasia Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Primary interstitial lung disease specific to adulthood Severe acute respiratory syndrome Dyskeratosis congenita Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency Severe combined immunodeficiency due to DCLRE1C deficiency Leukocyte adhesion deficiency type II T-B+ severe combined immunodeficiency due to gamma chain deficiency Primary immunodeficiency syndrome due to LAMTOR2 deficiency Leukocyte adhesion deficiency type I Severe combined immunodeficiency due to adenosine deaminase deficiency Juvenile polymyositis Apnea of prematurity Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency Combined immunodeficiency with granulomatosis Leukocyte adhesion deficiency type III Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome Dianzani autoimmune lymphoproliferative disease Pulmonary interstitial glycogenosis Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome Autoimmune lymphoproliferative syndrome with recurrent viral infections Sudden infant death-dysgenesis of the testes syndrome Interstitial lung disease Kawasaki disease Familial isolated congenital asplenia Secondary interstitial lung disease specific to adulthood associated with a systemic disease Pulmonary alveolar microlithiasis Takayasu arteritis Hyperzincemia and hypercalprotectinemia Pulmonary nodular lymphoid hyperplasia Pneumoconiosis Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency Recurrent infection due to specific granule deficiency Neuroendocrine cell hyperplasia of infancy Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Transient hypogammaglobulinemia of infancy Hepatic veno-occlusive disease-immunodeficiency syndrome Postinfectious vasculitis Langerhans cell histiocytosis specific to adulthood Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib Pearson syndrome Acute interstitial pneumonia Activated PI3K-delta syndrome Interstitial lung disease in childhood and adulthood Chronic respiratory distress with surfactant metabolism deficiency Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease Reactive arthritis Recurrent respiratory papillomatosis Immunodeficiency due to a classical component pathway complement deficiency Idiopathic bronchiectasis Lymphoid interstitial pneumonia Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Neonatal acute respiratory distress due to SP-B deficiency Idiopathic eosinophilic pneumonia Herpes simplex virus encephalitis Respiratory bronchiolitis-interstitial lung disease syndrome Autoinflammatory syndrome of childhood 22q11.2 deletion syndrome Hyper-IgM syndrome type 3 Immunodeficiency due to a late component of complement deficiency Combined immunodeficiency due to CARD11 deficiency Nakajo-Nishimura syndrome Hyper-IgM syndrome type 2 X-linked hyper-IgM syndrome Hyper-IgM syndrome type 5 Immunodeficiency due to MASP-2 deficiency Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency Hyper-IgM syndrome type 4 Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies T-B+ severe combined immunodeficiency due to JAK3 deficiency Immunodeficiency by defective expression of MHC class II T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency Nijmegen breakage syndrome-like disorder Eosinophilic fasciitis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Epidermodysplasia verruciformis Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency Muckle-Wells syndrome Cryoglobulinemic vasculitis Siegler-Brewer-Carey syndrome Constitutional neutropenia with extra-hematopoietic manifestations PLCG2-associated antibody deficiency and immune dysregulation Oligoarticular juvenile idiopathic arthritis Primary interstitial lung disease in childhood and adulthood Isolated agammaglobulinemia Chédiak-Higashi syndrome Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency Other immunodeficiency syndromes due to defects in innate immunity T-B- severe combined immunodeficiency Unspecified juvenile idiopathic arthritis Letterer-Siwe disease Omenn syndrome Systemic-onset juvenile idiopathic arthritis T-B+ severe combined immunodeficiency due to CD45 deficiency Hashimoto-Pritzker syndrome Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Adult pulmonary Langerhans cell histiocytosis Syndromic agammaglobulinemia Immunodeficiency due to ficolin3 deficiency T-B+ severe combined immunodeficiency Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta Combined immunodeficiency due to STK4 deficiency Cartilage-hair hypoplasia Familial spontaneous pneumothorax Roifman syndrome Cystic fibrosis Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome Polyarticular juvenile idiopathic arthritis X-linked severe congenital neutropenia Combined immunodeficiency due to ORAI1 deficiency X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency Combined immunodeficiency due to STIM1 deficiency Autoimmune polyendocrinopathy type 1 Diffuse alveolar hemorrhage Hereditary periodic fever syndrome Microscopic polyangiitis X-linked mendelian susceptibility to mycobacterial diseases NLRP12-associated hereditary periodic fever syndrome Kostmann syndrome Relapsing polychondritis Eosinophilic granulomatosis with polyangiitis Severe congenital neutropenia X-linked agammaglobulinemia Severe combined immunodeficiency due to DNA-PKcs deficiency Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells Blau syndrome Autoinflammatory syndrome with immune deficiency Hoyeraal-Hreidarsson syndrome Combined immunodeficiency with facio-oculo-skeletal anomalies Periodic fever syndrome of childhood Deficiency in anterior pituitary function-variable immunodeficiency syndrome Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Severe combined immunodeficiency due to complete RAG1/2 deficiency Mixed autoinflammatory and autoimmune syndrome Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Immunodeficiency with factor I anomaly Cohen syndrome Schimke immuno-osseous dysplasia Immunodeficiency due to absence of thymus Enthesitis-related juvenile idiopathic arthritis Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency Acute lung injury Interstitial lung disease specific to childhood Alpha-1-antitrypsin deficiency Laron syndrome with immunodeficiency 16q24.1 microdeletion syndrome Young syndrome Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder Pyogenic autoinflammatory syndrome of childhood Rare systemic or rheumatological disease of childhood Adult acute respiratory distress syndrome Syndrome with combined immunodeficiency X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency Primary immunodeficiency due to a defect in adaptive immunity Immunodeficiency with factor H anomaly Autoimmune pulmonary alveolar proteinosis Unclassified autoinflammatory syndrome of childhood Mendelian susceptibility to mycobacterial diseases Hypohidrotic ectodermal dysplasia with immunodeficiency House allergic alveolitis Primary interstitial lung disease specific to childhood Farmer's lung disease Occupational allergic alveolitis Sterile multifocal osteomyelitis with periostitis and pustulosis Familial Mediterranean fever Hyper-IgE syndrome Secondary interstitial lung disease in childhood and adulthood Pigeon-breeder lung disease Hyperimmunoglobulinemia D with periodic fever Infantile onset panniculitis with uveitis and systemic granulomatosis Granulomatous autoinflammatory syndrome of childhood Primary interstitial lung disease specific to childhood due to alveolar structure disorder Lichtenstein syndrome Recurrent Neisseria infections due to factor D deficiency Common variable immunodeficiency Infant acute respiratory distress syndrome Allergic bronchopulmonary aspergillosis Gorham-Stout disease Susceptibility to infection due to TYK2 deficiency Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease Cryptogenic organizing pneumonia FADD-related immunodeficiency Hereditary pulmonary alveolar proteinosis Tracheobronchopathia osteochondroplastica Severe combined immunodeficiency Meconium aspiration syndrome Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Bronchiolitis obliterans Idiopathic recurrent pericarditis Reticular dysgenesis Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Infantile apnea Autosomal dominant severe congenital neutropenia Hyper-IgM syndrome with susceptibility to opportunistic infections Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells Immunodeficiency due to selective anti-polysaccharide antibody deficiency Purine nucleoside phosphorylase deficiency Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency Immunoglobulin A vasculitis Unexplained periodic fever syndrome of childhood Overlapping connective tissue disease WHIM syndrome Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome Congenital alveolar capillary dysplasia Selective IgM deficiency Granulomatosis with polyangiitis Spondyloenchondrodysplasia Other immunodeficiency syndrome with predominantly antibody defects DNA repair defect other than combined T-cell and B-cell immunodeficiencies Primary interstitial lung disease specific to childhood due to alveolar vascular disorder Langerhans cell histiocytosis in childhood and adulthood Rare pediatric systemic disease Hyper-IgM syndrome without susceptibility to opportunistic infections Immunodeficiency by defective expression of MHC class I Idiopathic juvenile osteoporosis ICF syndrome Combined T and B cell immunodeficiency Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells Idiopathic CD4 lymphocytopenia Absent thumb-short stature-immunodeficiency syndrome Congenital chylothorax CINCA syndrome PFAPA syndrome Cernunnos-XLF deficiency Wiskott-Aldrich syndrome Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome Rare pediatric vasculitis Agammaglobulinemia Tumor necrosis factor receptor 1 associated periodic syndrome Immuno-osseous dysplasia Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome Combined immunodeficiency due to CD3gamma deficiency Secondary pulmonary hemosiderosis Juvenile idiopathic arthritis Immunodeficiency syndrome with autoimmunity Severe combined immunodeficiency due to CORO1A deficiency Combined immunodeficiency due to CD27 deficiency Congenital neutropenia-myelofibrosis-nephromegaly syndrome Isolated pulmonary capillaritis Drug-induced vasculitis Combined immunodeficiency due to ZAP70 deficiency Heiner syndrome Poikiloderma with neutropenia Staphylococcal necrotizing pneumonia Recurrent infections associated with rare immunoglobulin isotypes deficiency Idiopathic pulmonary hemosiderosis Congenital diaphragmatic hernia Immunodeficiency predominantly affecting antibody production Cyclic neutropenia Primary hemophagocytic lymphohistiocytosis Lymphoproliferative syndrome Immunodeficiency syndrome with hypopigmentation Pancytopenia due to IKZF1 mutations Congenital pulmonary lymphangiectasia Functional neutrophil defect T-cell immunodeficiency with epidermodysplasia verruciformis Hypersensitivity pneumonitis Proteasome-associated autoinflammatory syndrome Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease Hermansky-Pudlak syndrome due to AP-3 deficiency Idiopathic interstitial pneumonia Unclassified vasculitis X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia Griscelli syndrome type 2 Interstitial lung disease specific to infancy Combined pulmonary fibrosis-emphysema syndrome Neutropenia-monocytopenia-deafness syndrome Susceptibility to respiratory infections associated with CD8alpha chain mutation Combined immunodeficiency due to CRAC channel dysfunction Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Ataxia-telangiectasia Majeed syndrome Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis Constitutional neutropenia Nijmegen breakage syndrome Secondary interstitial lung disease specific to childhood associated with a systemic disease Properdin deficiency Immune dysregulation disease with immunodeficiency Unexplained long-lasting fever/inflammatory syndrome Anti-glomerular basement membrane disease Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency Cogan syndrome Combined immunodeficiency due to partial RAG1 deficiency Syndromic multisystem autoimmune disease due to Itch deficiency Leukocyte adhesion deficiency Autosomal agammaglobulinemia Desquamative interstitial pneumonia Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency Drug or radiation exposure-related interstitial lung disease Primary immunodeficiency due to a defect in innate immunity Severe dermatitis-multiple allergies-metabolic wasting syndrome Severe combined immunodeficiency due to FOXN1 deficiency RAS-associated autoimmune leukoproliferative disease Secondary interstitial lung disease specific to childhood associated with a connective tissue disease Sweet syndrome Chronic granulomatous disease Chronic mucocutaneous candidiasis Monocytopenia with susceptibility to infections

Provided care options 5

# Contact person
1
Kinderrheumatologische Ambulanz
Dr. med. Dr. Tilmann Kallinich

030 450566528
Website
Sprechzeiten nach Vereinbarung.

2
Christiane Herzog Zentrum, Mukoviszidose-Ambulanz
Prof. Dr. med. Mirjam Stahl

030 450566587
Email
Website
Sprechzeiten: Mo - Do 9:00 - 12:00 Uhr und 14:00 - 17:00 Uhr sowie Fr 9:00 - 12:00 Uhr nach Vereinbarung.

3
Spezialambulanz für chronisch nicht-bakterielle Osteomyelitis
Dr. Tilmann Kallinich

030 450566528
Website
Sprechzeiten nach Vereinbarung.

4
Immunologische Ambulanz
Prof. Dr. med. Horst von Bernuth

030 450566105
Email
Website
Sprechzeiten nach Vereinbarung.

5
Spezialambulanz für Allergologie und Pneumologie
Prof. Dr. med. Kirsten Beyer, Prof. Dr. Susanne Lau

030 450566556
Email
Website
Sprechzeiten nach Vereinbarung.

13.347380452.5422772Klinik für Pädiatrie mit Schwerpunkt Pneumologie, Immunologie und Intensivmedizin an der Charité Berlin
Last updated: 22.03.2023