se-atlas

Mapping of Health Care Providers
for People with Rare Diseases

Klinik für Kinder- und Jugendmedizin am Universitätsklinikum Ulm

Decription of facility

Director / Spokesperson
Prof. Dr. Klaus-Michael Debatin
Information
Care facility for children
Decription

Die 400 Mitarbeiterinnen und Mitarbeiter der Klinik für Kinder- und Jugendmedizin stellen mit großem Einsatz rund um die Uhr die umfassende und hochwertige universitätsmedizinische Versorgung von Kindern und Jugendlichen aller Altersgruppen sicher. Dazu stehen den Patienten 117 Betten, eine 24-Stunden-Notfallabulanz, eine Allgemeinambulanz sowie zahlreiche Spezialambulanzen zur Verfügung. Die Sektion Kinderchirurgie der Klinik für Allgemein- und Viszeralchirurgie hält weitere 14 Betten für die operative Versorgung vor. In einem breiten Angebot kümmert sich das Klinikteam auch um die notwendige Betreuung und Beratung während des Aufenthalts und in der Zeit danach. Das Team setzt sich dafür ein, auf der Basis neuster Diagnose- und Therapiekonzepte für jeden Patienten die beste Behandlung zu gewährleisten. Dazu trägt auch die international renommierte Forschung bei.

Care provisions

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

Contact

Prof. Dr. med. Klaus-Michael Debatin
0731 50057001
0731 50057002
klaus-michael.debatin@uniklinik-ulm.de
Website

http://www.uniklinik-ulm.de/struktur/kliniken/kinder-und-jugendmedizin.html

Address

Eythstraße 24
89075 Ulm

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Certificates 4

Preview of the assigned diseases 8

PEHO syndrome Immunodeficiency due to a complement cascade protein anomaly Von Willebrand disease type 3 Acute promyelocytic leukemia Cryopyrin-associated periodic syndrome Bartter syndrome Primary immunodeficiency Pyogenic arthritis-pyoderma gangrenosum-acne syndrome Subependymal giant cell astrocytoma Rare epilepsy Beckwith-Wiedemann syndrome Short-limb skeletal dysplasia with severe combined immunodeficiency Multiple intestinal atresia Schwartz-Jampel syndrome Moynahan syndrome Severe hemophilia B Glomerular disease Miller-Dieker syndrome Graft versus host disease Oculocerebrorenal syndrome of Lowe Mild hemophilia B Genetic susceptibility to infections due to particular pathogens Kleefstra syndrome due to 9q34 microdeletion Moderately severe hemophilia B Severe hemophilia A Lupus erythematosus panniculitis Isolated osteopoikilosis Spondyloepiphyseal dysplasia tarda Hemophilia B Hemophilia A Moderately severe hemophilia A Chronic cutaneous lupus erythematosus Neonatal lupus erythematosus Acute myeloid leukemia with t(8;16)(p11;p13) translocation Mild hemophilia A Rare gastroenterologic disease Autoimmune polyendocrinopathy type 2 DITRA Primary hyperoxaluria Wolf-Hirschhorn syndrome Dysosteosclerosis Cortical dysplasia-focal epilepsy syndrome Oculocerebrocutaneous syndrome Oligoastrocytoma Rasmussen subacute encephalitis Acute myeloid leukemia with t(8;21)(q22;q22) translocation Dendritic cell sarcoma not otherwise specified Precursor T-cell acute lymphoblastic leukemia Tick-borne encephalitis T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency Hypophosphatasia DEND syndrome Melnick-Needles syndrome Primary immunodeficiency with predisposition to severe viral infection PLCG2-associated antibody deficiency and immune dysregulation Melorheostosis Oligoarticular juvenile idiopathic arthritis Other immunodeficiency syndromes due to defects in innate immunity Unspecified juvenile idiopathic arthritis Inherited acute myeloid leukemia Duplication/inversion 15q11 Benign familial infantile epilepsy Isovaleric acidemia Systemic-onset juvenile idiopathic arthritis Infantile spasms-broad thumbs syndrome Familial partial epilepsy Astroblastoma Benign familial neonatal-infantile seizures Paroxysmal nocturnal hemoglobinuria Gray platelet syndrome Hemophilia Polyarticular juvenile idiopathic arthritis Cystic fibrosis Epilepsy-telangiectasia syndrome Severe combined immunodeficiency due to DNA-PKcs deficiency Autosomal dominant polycystic kidney disease Acute myeloid leukemia with CEBPA somatic mutations Autoinflammatory syndrome with immune deficiency Osteomesopyknosis Autosomal recessive polycystic kidney disease High-grade astrocytoma Osteopathia striata-cranial sclerosis syndrome Psoriasis-related juvenile idiopathic arthritis Neonatal epilepsy syndrome Enthesitis-related juvenile idiopathic arthritis Childhood-onset epilepsy syndrome Juvenile xanthogranuloma Dent disease type 1 Infantile epilepsy syndrome Small cell lung cancer Adolescent-onset epilepsy syndrome Syndrome with combined immunodeficiency Primary immunodeficiency due to a defect in adaptive immunity Alport syndrome Rare hematologic disease Familial hyperinsulinism Tetrasomy 12p Epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Symptomatic form of hemophilia A in female carriers Neurocutaneous syndrome with epilepsy Angelman syndrome Kimura disease Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Reticular dysgenesis Ring chromosome 14 syndrome W syndrome Monogenic disease with epilepsy Giant cell glioblastoma Symptomatic form of hemophilia B in female carriers Acute myeloid leukemia with recurrent genetic anomaly Buschke-Ollendorff syndrome Cerebral malformation with epilepsy Ring chromosome 20 syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Pycnodysostosis Chronic graft versus host disease Metabolic diseases with epilepsy Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) Acute graft versus host disease Anaplastic astrocytoma PHACE syndrome Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Aromatase excess syndrome Dermatomyositis Von Willebrand disease Gitelman syndrome Acute myeloid leukemia with 11q23 abnormalities Diffuse astrocytoma Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Combined T and B cell immunodeficiency Acute undifferentiated leukemia Cerebral diseases of vascular origin with epilepsy Von Willebrand disease type 1 Glioblastoma Unclassified acute myeloid leukemia Familial glucocorticoid deficiency Inflammatory and autoimmune disease with epilepsy Acute biphenotypic leukemia Low-grade astrocytoma Bilineal acute leukemia Fragile X syndrome Infectious disease with epilepsy Von Willebrand disease type 2 Juvenile idiopathic arthritis Protoplasmic astrocytoma Immunodeficiency predominantly affecting antibody production Astrocytoma Fibrillary astrocytoma Acute panmyelosis with myelofibrosis Rhabdomyosarcoma Ependymoblastoma Ataxia-telangiectasia Acute myeloid leukemia and myelodysplastic syndromes related to radiation Simpson-Golabi-Behmel syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Immune dysregulation disease with immunodeficiency Therapy related acute myeloid leukemia and myelodysplastic syndrome Quantitative and/or qualitative congenital phagocyte defect Gemistocytic astrocytoma Acute basophilic leukemia Pilocytic astrocytoma Neonatal inflammatory skin and bowel disease Primary immunodeficiency due to a defect in innate immunity Acute monoblastic leukemia Medulloepithelioma of the central nervous system Acute leukemia of ambiguous lineage Melorheostosis with osteopoikilosis Chronic granulomatous disease PEHO-like syndrome

Provided care options 10

# Contact person
1
Epilepsie-Ambulanz
Dr. med. Benedikt Winter

0731 50057010
Email
Website
Sprechzeiten nach Vereinbarung.

2
Onkologische Tagesklinik
Prof. Dr. med. Klaus-Michael Debatin, Prof. Dr. Holger Cario

0731 50057219
Email
Website
Sprechzeiten nach Vereinbarung.

3
Spezialambulanz für Mukoviszidose
Prof. Dr. M. Leichsenring

0731 50057292
Website
Sprechzeiten nach Vereinbarung.

4
Spezialambulanz Hämatologie
Prof. Dr. H. Cario

0731 50057330
Email
Website
Sprechzeiten: Di 08:30 - 11:30 Uhr.

5
Spezialambulanz Hämostaseologie (Gerinnungsstörungen)
Prof. Dr. H. Cario

0731 50057330
Email
Website
Sprechzeiten: Mi 8:30 - 12:00 Uhr.

6
Spezialambulanz Rheumatologie und Autoimmunerkrankungen
Prof. Dr. Ansgar Schulz

0731 50057275
Email
Website
Sprechzeiten: Mi 8:30 - 16:00 Uhr, Do 14:00 - 16:00 Uhr und nach Vereinbarung..

7
Spezialsprechstunde für angeborene Immundefekte
Prof. Dr. Ansgar Schulz, Dr. Manfred Hönig

0731 50057271
Email
Website
Sprechzeiten nach Vereinbarung.
This consultation offers genetic counselling.

8
Spezialsprechstunde für Nierenerkrankungen im Kindesalter
Dr. med. Ortraud Beringer

0731 50057330
Email
Website
Sprechzeiten: Mo, Mi 8:00 - 12:00 Uhr und 13:30 - 15:00 Uhr.

9
Spezialsprechstunde für Osteopetrose
Prof. Dr. med. Ansgar Schulz

0731 50057154
Email
Website
Sprechzeiten nach Vereinbarung.

10
WHIM-Syndrom Sprechstunde
Prof. Dr. Ansgar Schulz, Prof. Dr. Badolato Raffaele, Dr. Jean Donadieu

0731 50057271
Email
Website
Sprechzeiten nach Vereinbarung.
This consultation offers genetic counselling.

9.9927268767211948.410931237931884Klinik für Kinder- und Jugendmedizin am Universitätsklinikum Ulm
Last updated: 03.11.2020