SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik und Poliklinik für Dermatologie am Universitätsklinikum Dresden

Description of facility

Director / Spokesperson
Prof. Dr. med. Stefan Beissert
Information
Care facility for adults and children
Description
Insbesondere Erkrankungen der Haut und Allergien gehören zu den häufigsten Erkrankungen in unserer Gesellschaft. Die Hautklinik ist auf breiter Basis in Forschung, Lehre und Krankenversorgung aufgestellt. Ziel ist es, durch Forschung und Krankenversorgung vor Ort das Wissen um die Entstehung von Hautkrankheiten sowie Allergien zu verbessern. Dadurch können moderne effektive sowie nebenwirkungsarme Therapien entwickelt werden. Die Klinik bemüht sich, die vielfältigen Aktivitäten transparent darzustellen und Sie über die aktuellen Entwicklungen zu informieren.

Care provisions

This facility offers the following
  • Clinical studies / research
  • Diagnostic
  • Therapy

Contact

Prof. Dr. med. Stefan Beissert
0351 4582497
0351 4584338
dermatologie@uniklinikum-dresden.de
Website https://www.uniklinikum-dresden.de/de/das-klinikum/kliniken-polikliniken-institute/der

Address

Fetscherstraße 74
01307 Dresden

Calculate route

Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Preview of the assigned diseases 4

Acquired angioedema Rare urticaria Epidermolysis bullosa simplex with anodontia/hypodontia Typical urticaria pigmentosa Nodular urticaria pigmentosa Systemic mastocytosis Plaque-form urticaria pigmentosa Drug reaction with eosinophilia and systemic symptoms Epidermolysis bullosa simplex with mottled pigmentation Smoldering systemic mastocytosis Autosomal dominant generalized epidermolysis bullosa simplex, severe form Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement PLCG2-associated antibody deficiency and immune dysregulation Intermediate generalized junctional epidermolysis bullosa Isolated bone marrow mastocytosis Localized epidermolysis bullosa simplex Severe generalized junctional epidermolysis bullosa Junctional epidermolysis bullosa with pyloric atresia Localized junctional epidermolysis bullosa Late-onset junctional epidermolysis bullosa Junctional epidermolysis bullosa inversa Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form Melkersson-Rosenthal syndrome Localized dystrophic epidermolysis bullosa, pretibial form Muckle-Wells syndrome Dystrophic epidermolysis bullosa Recessive dystrophic epidermolysis bullosa inversa Lymphoadenopathic mastocytosis with eosinophilia Epidermolysis bullosa simplex Self-improving dystrophic epidermolysis bullosa Junctional epidermolysis bullosa Suprabasal epidermolysis bullosa simplex Classic mast cell leukemia Basal epidermolysis bullosa simplex Aleukemic mast cell leukemia Kindler epidermolysis bullosa Ectodermal dysplasia-skin fragility syndrome Localized dystrophic epidermolysis bullosa, acral form Localized dystrophic epidermolysis bullosa, nails only Epidermolysis bullosa simplex with circinate migratory erythema Lethal acantholytic erosive disorder Epidermolysis bullosa simplex with pyloric atresia Hereditary angioedema type 1 Cutaneous mastocytoma Maculopapular cutaneous mastocytosis Hereditary angioedema type 2 Diffuse cutaneous mastocytosis F12-related hereditary angioedema with normal C1Inh Acquired angioedema type 1 Acquired angioedema type 2 Renin-angiotensin-aldosterone system-blocker-induced angioedema Bullous diffuse cutaneous mastocytosis Laryngo-onycho-cutaneous syndrome Cutaneous mastocytosis Mastocytosis Autosomal recessive generalized epidermolysis bullosa simplex Junctional epidermolysis bullosa, non-Herlitz type Epidermolysis bullosa simplex superficialis Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form Centripetalis recessive dystrophic epidermolysis bullosa Pruritic urticarial papules and plaques of pregnancy Pseudoxanthomatous diffuse cutaneous mastocytosis Telangiectasia macularis eruptiva perstans Dystrophic epidermolysis bullosa pruriginosa Indolent systemic mastocytosis Aggressive systemic mastocytosis Extracutaneous mastocytoma Systemic mastocytosis with associated hematologic neoplasm Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Mast cell sarcoma Schnitzler syndrome Mast cell leukemia Non-histaminic angioedema Autosomal dominant generalized dystrophic epidermolysis bullosa Inherited epidermolysis bullosa Epidermolysis bullosa simplex with muscular dystrophy Familial cold urticaria Hereditary angioedema

Provided care options 3

# Contact person
1
Lasersprechstunde
Dr. Roland Aschoff, Dr. Ulrike Proske

0351 4582012
Email
Website
Sprechzeiten: Mo 8:00 – 11:00 Uhr und 14:00 – 16:30 Uhr, Di 14:00 – 17:00 Uhr, Mi 8:00 – 11:00 Uhr, Do 8:00 – 12:00 Uhr und 14:00 – 17:00 Uhr sowie Fr 10:00 – 10:30 Uhr nach Vereinbarung.

2
Sprechstunde für Urtikaria, Angioödem und Mastozytose
Prof. Dr. Andrea Bauer

0351 4582947
Email
Website
Sprechzeiten: Mo - Fr 7:30 - 12:00 Uhr sowie Mo und Do 14:00 - 17:00 Uhr nach Vereinbarung.

3
Spezialambulanz für Autoimmundermatosen, hereditäre Epidermolysen
Prof. Dr. Claudia Günther

0351 4582007
Email
Website
Sprechzeiten: Di 8:00 - 12:00 Uhr, Do 9:00 - 13:00 Uhr.

13.77960419635201351.054337375077196Klinik und Poliklinik für Dermatologie am Universitätsklinikum Dresden
Last updated: 29.12.2022