Mapping of Health Care Providers
for People with Rare Diseases

Zentrum für Seltene Hauterkrankungen am Universitätsklinikum Tübingen

Decription of facility

Director / Spokesperson
Dr. Stephan Forchhammer
Care facility for adults and children

Das Zentrum für Seltene Hauterkrankungen (ZSH) ist ein Unterzentrum des ZSE Tübingens, das an dem Universitätsklinikum Tübingen angesiedelt ist. Zu dem am ZSH beteiligten Kliniken und Abteilungen gehören die Universitätshautklinik, das Institut für Humangenetik, die Abteilung für Medizinische Genetik, die Universitätsaugenklinik, die Klinik für Kinder- und Jugendmedizin, das Zentrum für Neurologie, die Radiologische Universitätsklinik, die Abteilung für Diagnostische und Interventionelle Neuroradiologie, die Universitätsklinik für Zahn-, Mund- und Kieferheilkunde, die Prothetische Abteilung, die Innere Medizin II/Hämatologie Onkologie und das Institut für Pathologie. Folgende seltene Erkrankungen und Krankheitsgruppen werden hier behandelt: Ektodermale Dysplasie, Seltene kutane Lymphome, Autoinflammationssyndrome, Seltene Autoimmunkrankheiten, Sklerodermie, Mastozytose und Kongenitale Melanozytäre Nävi.

Care provisions

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


Dr. Stephan Forchhammer
07071 2987692


Liebermeisterstraße 25
72076 Tübingen

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Preview of the assigned diseases 8

Epidermolysis bullosa simplex due to exophilin 5 deficiency Indolent primary cutaneous T-cell lymphoma Cataract-hypertrichosis-intellectual disability syndrome Trichorhinophalangeal syndrome Plaque-form urticaria pigmentosa Aggressive primary cutaneous T-cell lymphoma Marshall syndrome Cranioectodermal dysplasia Nodular urticaria pigmentosa Autoimmune bullous skin disease Epidermolysis bullosa simplex, generalized severe Ellis Van Creveld syndrome Teebi-Shaltout syndrome Epidermolysis bullosa simplex with mottled pigmentation Indolent primary cutaneous B-cell lymphoma Dermatitis herpetiformis Localized epidermolysis bullosa simplex Aggressive primary cutaneous B-cell lymphoma Dermatoosteolysis, Kirghizian type Epidermolysis bullosa simplex, generalized intermediate Bullous pemphigoid Junctional epidermolysis bullosa, generalized intermediate GAPO syndrome Epidermolysis bullosa simplex, Ogna type Orofaciodigital syndrome type 1 Pemphigus vulgaris Localized junctional epidermolysis bullosa, non-Herlitz type Trichodysplasia-amelogenesis imperfecta syndrome Dermoodontodysplasia ADULT syndrome Junctional epidermolysis bullosa, generalized severe Sparse hair-short stature-skin anomalies syndrome Junctional epidermolysis bullosa inversa Xeroderma pigmentosum-Cockayne syndrome complex Junctional epidermolysis bullosa-pyloric atresia syndrome Sézary syndrome Ito hypomelanosis Pili torti-onychodysplasia syndrome SHORT syndrome Mandibular hypoplasia-deafness-progeroid syndrome Late-onset junctional epidermolysis bullosa Focal facial dermal dysplasia type I Pilodental dysplasia-refractive errors syndrome Recessive dystrophic epidermolysis bullosa inversa Severe generalized recessive dystrophic epidermolysis bullosa Primary cutaneous B-cell lymphoma Cockayne syndrome type 2 Dystrophic epidermolysis bullosa Transient bullous dermolysis of the newborn Cockayne syndrome type 1 Epidermolysis bullosa simplex Pretibial dystrophic epidermolysis bullosa Junctional epidermolysis bullosa Cockayne syndrome type 3 Mycosis fungoides and variants Ectodermal dysplasia-blindness syndrome Paraneoplastic pemphigus Focal facial dermal dysplasia type III Focal facial dermal dysplasia Böök syndrome Hidrotic ectodermal dysplasia, Christianson-Fourie type Suprabasal epidermolysis bullosa simplex Chondroectodermal dysplasia with night blindness Hidrotic ectodermal dysplasia, Halal type Amelocerebrohypohidrotic syndrome Tricho-retino-dento-digital syndrome Autosomal dominant hypohidrotic ectodermal dysplasia Hypertrichosis cubiti Cartilage-hair hypoplasia Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome Hypertrichosis lanuginosa congenita Basal epidermolysis bullosa simplex Dermatopathia pigmentosa reticularis AREDYLD syndrome Epidermolysis bullosa simplex due to plakophilin deficiency Hereditary acrokeratotic poikiloderma, Weary type Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Non-Langerhans cell histiocytosis Kindler syndrome Lacrimoauriculodentodigital syndrome Focal facial dermal dysplasia type II X-linked hypohidrotic ectodermal dysplasia Rothmund-Thomson syndrome Ectodermal dysplasia, trichoodontoonychial type Wiedemann-Rautenstrauch syndrome Hypodontia-dysplasia of nails syndrome Systemic disease with skin involvement Lelis syndrome Multicentric reticulohistiocytosis Focal dermal hypoplasia Genetic photodermatosis Acral dystrophic epidermolysis bullosa Progeroid syndrome Generalized eruptive histiocytosis Gorlin-Chaudhry-Moss syndrome Acroosteolysis-keloid-like lesions-premature aging syndrome Primary cutaneous T-cell lymphoma Alopecia-contractures-dwarfism-intellectual disability syndrome Rothmund-Thomson syndrome type 1 Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome Autoinflammatory syndrome with skin involvement Xeroderma pigmentosum variant Hidrotic ectodermal dysplasia Incontinentia pigmenti Dominant dystrophic epidermolysis bullosa, nails only Cockayne syndrome Autosomal dominant palmoplantar keratoderma and congenital alopecia Epidermolysis bullosa simplex with circinate migratory erythema Corneodermatoosseous syndrome Juvenile xanthogranuloma Hutchinson-Gilford progeria syndrome Benign cephalic histiocytosis Hypohidrotic ectodermal dysplasia Xanthoma disseminatum Trichorhinophalangeal syndrome type 1 and 3 Rothmund-Thomson syndrome type 2 Hallermann-Streiff syndrome Curly hair-acral keratoderma-caries syndrome Epidermolysis bullosa simplex with pyloric atresia Dahlberg-Borer-Newcomer syndrome Hereditary acrokeratotic poikiloderma of Kindler-Weary CHIME syndrome Hypohidrotic ectodermal dysplasia with immunodeficiency Papular xanthoma Cronkhite-Canada syndrome Toriello-Lacassie-Droste syndrome Lethal acantholytic epidermolysis bullosa Focal facial dermal dysplasia type IV Drug-induced lupus erythematosus KID syndrome Congenital generalized hypertrichosis, Ambras type Infantile onset panniculitis with uveitis and systemic granulomatosis Pure hair and nail ectodermal dysplasia Odonto-tricho-ungual-digito-palmar syndrome Schöpf-Schulz-Passarge syndrome Choroidal atrophy-alopecia syndrome Ectodermal dysplasia with natal teeth, Turnpenny type Hartnup disease Necrobiotic xanthogranuloma Limb-mammary syndrome Hypotrichosis with juvenile macular degeneration Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Generalized pustular psoriasis UV-sensitive syndrome Ameloonychohypohidrotic syndrome Naegeli-Franceschetti-Jadassohn syndrome Cleft lip/palate-ectodermal dysplasia syndrome Diffuse cutaneous mastocytosis Cutaneous mastocytoma Trichodental syndrome Maculopapular cutaneous mastocytosis Tricho-dento-osseous syndrome Indeterminate cell histiocytosis Trichodermodysplasia-dental alterations syndrome Large congenital melanocytic nevus Kein Name gefunden Hereditary progressive mucinous histiocytosis Trichoodontoonychial dysplasia Cerebellar ataxia-ectodermal dysplasia syndrome Deafness-enamel hypoplasia-nail defects syndrome Progressive nodular histiocytosis Autosomal dominant trichoodontoonychodysplasia-syndactyly Werner syndrome Trichothiodystrophy Cutaneous mastocytosis Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Blepharo-cheilo-odontic syndrome Bullous diffuse cutaneous mastocytosis Erdheim-Chester disease LOC syndrome Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Xeroderma pigmentosum Epidermolysis bullosa simplex, autosomal recessive K14 Trichorhinophalangeal syndrome type 2 Deafness-onychodystrophy syndrome Centripetalis recessive dystrophic epidermolysis bullosa Progeria-short stature-pigmented nevi syndrome Epidermolysis bullosa simplex superficialis Junctional epidermolysis bullosa, non-Herlitz type Atypical Werner syndrome Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome Dystrophic epidermolysis bullosa pruriginosa Pseudoxanthomatous diffuse cutaneous mastocytosis Reynolds syndrome Recessive dystrophic epidermolysis bullosa, generalized intermediate Pemphigus vegetans Dubowitz syndrome Leprechaunism Conductive deafness-ptosis-skeletal anomalies syndrome Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Telangiectasia macularis eruptiva perstans Pemphigus foliaceus Pemphigus erythematosus COFS syndrome Ogden syndrome Pyramidal molars-abnormal upper lip syndrome Fried's tooth and nail syndrome Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Pellagra-like skin rash-neurological manifestations syndrome Ectodermal dysplasia-sensorineural deafness syndrome Pyogenic arthritis-pyoderma gangrenosum-acne syndrome Autosomal recessive hypohidrotic ectodermal dysplasia Anonychia with flexural pigmentation Cardiofaciocutaneous syndrome Superficial pemphigus Generalized dominant dystrophic epidermolysis bullosa Mucous membrane pemphigoid Acquired epidermolysis bullosa Herpetiform pemphigus Linear IgA dermatosis Zlotogora-Ogur syndrome X-linked congenital generalized hypertrichosis Schinzel-Giedion syndrome Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Gingival fibromatosis-hypertrichosis syndrome Inherited epidermolysis bullosa Oculodentodigital dysplasia Scleroderma DOORS syndrome Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Contractures-ectodermal dysplasia-cleft lip/palate syndrome Autosomal dominant deafness-onychodystrophy syndrome Pseudoprogeria syndrome Epidermolysis bullosa simplex with muscular dystrophy Oculoosteocutaneous syndrome Dermotrichic syndrome Diffuse cutaneous systemic sclerosis EEC syndrome Cooks syndrome EEM syndrome Bloom syndrome Pemphigoid gestationis Scalp-ear-nipple syndrome Oculotrichodysplasia Ectodermal dysplasia syndrome Porphyria cutanea tarda Limited cutaneous systemic sclerosis Odonto-onycho-dermal dysplasia Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Odonto-onycho dysplasia-alopecia syndrome Adult T-cell leukemia/lymphoma Odontotrichomelic syndrome Primary cutaneous CD30+ T-cell lymphoproliferative disease Papillon-Lefèvre syndrome Primary cutaneous lymphoma Johanson-Blizzard syndrome Acrofacial dysostosis, Weyers type Johnson neuroectodermal syndrome CREST syndrome Mandibuloacral dysplasia with type B lipodystrophy Localized scleroderma EEC syndrome and related syndrome Ectodermal dysplasia-syndactyly syndrome Extranodal nasal NK/T cell lymphoma Primary cutaneous gamma/delta-positive T-cell lymphoma Mandibuloacral dysplasia with type A lipodystrophy Primary cutaneous follicle center lymphoma Systemic sclerosis Dyskeratosis congenita Mandibuloacral dysplasia Autosomal recessive palmoplantar keratoderma and congenital alopecia Primary cutaneous peripheral T-cell lymphoma not otherwise specified Primary cutaneous marginal zone B-cell lymphoma Taurodontia-absent teeth-sparse hair syndrome Subcutaneous panniculitis-like T-cell lymphoma Epidermolysis bullosa simplex due to BP230 deficiency Typical urticaria pigmentosa Primary cutaneous diffuse large B-cell lymphoma, leg type Epidermolysis bullosa simplex with anodontia/hypodontia Bartsocas-Papas syndrome Ectodermal dysplasia-cutaneous syndactyly syndrome Neurocutaneous melanocytosis Familial porphyria cutanea tarda Sporadic porphyria cutanea tarda

Provided care options 0

No available care options have been entered.
9.0525538901714148.52602844348741Zentrum für Seltene Hauterkrankungen am Universitätsklinikum Tübingen
Last updated: 08.09.2020