se-atlas

Mapping of Health Care Providers
for People with Rare Diseases

Interdisziplinäres Zentrum für seltene und genetische Hautkrankheiten am LMU Klinikum München

Decription of facility

Director / Spokesperson
Prof. Dr. med. Kathrin Giehl
Information
Care facility for adults and children
Decription

Im Herbst 2011 wurde das Interdisziplinäre Zentrum für seltene und genetische Hautkrankheiten gegründet. Ziel des Zentrums ist es, Menschen mit genetischen und seltenen Hautkrankheiten nach dem neuesten Stand der Wissenschaft zu behandeln, kompetent interdisziplinär zu betreuen und durch gemeinsame Forschungsaktivitäten die Möglichkeit der Behandlung zu erweitern. Mit Gründung des interdisziplinären Zentrums für seltene und genetische Hautkrankheiten wird eine Plattform für interdisziplinäre Fallbesprechungen, Fortbildungen und Informationsaustausch angeboten. Die behandelnden Ärzte sollen in der interdisziplinären Patientenbetreuung unterstützt und die Betroffenen umfassend und qualitativ hochwertig medizinisch betreut werden. Alle drei Monate werden Patienten mit speziellen Krankheitsbildern in interdisziplinären Fallkonferenzen vorgestellt. Innerhalb des Interdisziplinären Zentrums für seltene und genetische Hautkrankheiten werden in der Dermatologischen Klinik Spezialsprechstunden angeboten, in denen Spezialisten für die entsprechenden Krankheitsgruppen zielgerichtete diagnostische und therapeutische Maßnahmen etabliert haben und interdisziplinär kooperieren. Diese Spezialsprechstunden werden angeboten für: Genodermatosen, bullöse Autoimmunkrankheiten, Kollagenosen, Birt-Hogg-Dubé Syndrom, kutane Lymphome, Autoinflammationssyndrome, Mastozytose, seltene Haarerkrankungen und seltene Hauttumoren. Nähere Informationen zu den einzelnen Sprechstunden unter "Versorgungsangebote".

Consultation hours

Special consultation hours:
Terminvereinbarung und Information für spezielle Ambulanzen oder Spezialsprechstunden unter 089 440056391 oder über E-Mail unter: kathrin.giehl@med.uni-muenchen.de.

Care provisions

This facility offers the following
  • Participation in registries
    Lokale Register: disseminierte juvenile Xanthogranulome, Palmoplantarkeratosen, Pili annulati, Golz Gorlin, Birt-Hogg-Dubé, Mastozytose, Rosazea fulminans, Akne inversa. Nationale Register: disseminierte juvenile Xanthogranulome, Ichthyosen und Palmoplantarkeratosen (NIRK), Merkelzell Karzinom, Systemische Sklerodermie mit digitalen Ulzerationen. Internationale Register: Systemische Sklerodermie
  • Genetic counselling
  • Clinical studies / research
    - Netherton Syndrom: phänotypische Varianz und Therapieeinfluß; - Molekulargenetische Untersuchungen von Palmoplantarkeratosen;
    - Molekulargenetische Untersuchungen bei der Haarschaftanomalie Pili annulati; - Birt Hogg-Dubé: Genotyp-Phänotyp-Korrelation und Exploration assoziierter Neoplasien, insbesondere dem malignen Melanom;
    -Disseminierte und systemische juvenile Xanthogranulome - Erforschung der Pathogenese und Phänotypbestimmung
  • Diagnostic
  • Therapy
  • Contact person for patients with an unclear diagnosis
    Das Zentrum bietet eine ausführliche Diagnostik bei Patienten mit unklarer Diagnose an.
  • Contact with support groups
    Selbsthilfe Ichthyose e.V. Deutschland, Tuberöse Sklerose Deutschland e.V., Sklerodermie Selbsthilfe e.V., Selbsthilfegruppe Ektodermale Dysplasie e.V.

Contact

Prof. Dr. med. Kathrin Giehl
089 440056391
089 440056202
kathrin.giehl@med.uni-muenchen.de
Website

http://www.klinikum.uni-muenchen.de/Interdisziplinaeres-Zentrum-fuer-genetische-und-seltene-Hautkrankheiten/de/index.html

Address

Frauenlobstrasse 9 - 11
80337 München

Campus Innenstadt; Klinik und Poliklinik für Dermatologie und Allergologie

Calculate route

Languages

Germany.png Deutsch
United_Kingdom.png Englisch

European Reference Network 1

Mentioned by the following facilities 1

Preview of the assigned diseases 13

Hereditary hypotrichosis with recurrent skin vesicles Papillon-Lefèvre syndrome Ulerythema ophryogenesis Chronic cutaneous lupus erythematosus Keratinopathic ichthyosis Johanson-Blizzard syndrome MEDNIK syndrome Extranodal nasal NK/T cell lymphoma Primary cutaneous lymphoma Malignant atrophic papulosis Primary cutaneous marginal zone B-cell lymphoma Acrofacial dysostosis, Weyers type Infantile digital fibromatosis Johnson neuroectodermal syndrome Focal palmoplantar keratoderma Brain-lung-thyroid syndrome Limited systemic sclerosis Autosomal ichthyosis syndrome with fatal disease course CREST syndrome Peeling skin syndrome Ectodermal dysplasia-syndactyly syndrome FLOTCH syndrome EEC syndrome and related syndrome Genetic porokeratosis Infantile myofibromatosis Primary cutaneous gamma/delta-positive T-cell lymphoma Hyperkeratosis lenticularis perstans Ectodermal dysplasia-cutaneous syndactyly syndrome Primary cutaneous follicle center lymphoma Flynn-Aird syndrome Genetic hair anomaly Systemic sclerosis Rare nevus Dyskeratosis congenita Autosomal recessive palmoplantar keratoderma and congenital alopecia Genetic epidermal appendage anomaly Lymphedema CHILD syndrome Primary cutaneous peripheral T-cell lymphoma not otherwise specified Taurodontia-absent teeth-sparse hair syndrome Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome Autosomal dominant multiple pterygium syndrome Barber-Say syndrome Autosomal ichthyosis syndrome with prominent neurologic signs LMNA-related cardiocutaneous progeria syndrome Subcutaneous panniculitis-like T-cell lymphoma Typical urticaria pigmentosa White sponge nevus Peutz-Jeghers syndrome Rare skin tumor or hamartoma Hypotrichosis simplex Familial multiple lipomatosis Angora hair nevus Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome Unclassified genetic skin disorder Epidermolysis bullosa simplex with anodontia/hypodontia Genetic nail anomaly Primary cutaneous diffuse large B-cell lymphoma, leg type Bartsocas-Papas syndrome Isolated focal palmoplantar keratoderma Van den Bosch syndrome Generalized eruptive keratoacanthoma Disease with diffuse palmoplantar keratoderma as a major feature Multiple self-healing squamous epithelioma Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome Familial angiolipomatosis Tyrosinemia type 2 Autosomal ichthyosis syndrome with other associated signs Phakomatosis pigmentokeratotica Nodular urticaria pigmentosa Premature aging Indolent primary cutaneous T-cell lymphoma Phakomatosis pigmentovascularis Cataract-hypertrichosis-intellectual disability syndrome Hypertrichosis-acromegaloid facial appearance syndrome Gardner syndrome Systemic mastocytosis Autosomal dominant isolated diffuse palmoplantar keratoderma Plaque-form urticaria pigmentosa Ehlers-Danlos syndrome, hypermobility type Epidermolysis bullosa simplex due to BP230 deficiency Malignant melanoma of the mucosa Scleromyxedema Rare genetic skin disease Congenital non-bullous ichthyosiform erythroderma Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature Ehlers-Danlos syndrome, vascular type Smouldering systemic mastocytosis Genetic pigmentation anomaly of the skin Ehlers-Danlos syndrome, classic type Dermatofibrosarcoma protuberans Marshall syndrome Cranioectodermal dysplasia Scalp disease Nestor-Guillermo progeria syndrome Genetic sebaceous gland anomaly Parkes Weber syndrome ANE syndrome Self-improving collodion baby Epidermolysis bullosa simplex, generalized severe Klippel-Trénaunay syndrome Autoimmune bullous skin disease Palmoplantar keratoderma-esophageal carcinoma syndrome Ellis Van Creveld syndrome McCune-Albright syndrome Aggressive primary cutaneous T-cell lymphoma Keratoderma hereditarium mutilans with ichthyosis Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature Epidermolytic palmoplantar keratoderma Genetic hyperpigmentation of the skin Epidermolysis bullosa simplex due to exophilin 5 deficiency Teebi-Shaltout syndrome Focal palmoplantar and gingival keratoderma Autosomal recessive disease with focal palmoplantar keratoderma as a major feature Alopecia totalis Indolent primary cutaneous B-cell lymphoma Epidermolysis bullosa simplex with mottled pigmentation Non-epidermolytic palmoplantar keratoderma Palmoplantar keratoderma-spastic paralysis syndrome Autosomal recessive isolated diffuse palmoplantar keratoderma Ehlers-Danlos syndrome type 1 Alopecia universalis Dermatitis herpetiformis Isolated punctate palmoplantar keratoderma Localized epidermolysis bullosa simplex Aggressive primary cutaneous B-cell lymphoma Primary non-essential cutis verticis gyrata Linear verrucous nevus syndrome Piebaldism Palmoplantar keratoderma-deafness syndrome Epidermolysis bullosa simplex, Ogna type Didymosis aplasticosebacea Dermatoosteolysis, Kirghizian type Keratosis follicularis-dwarfism-cerebral atrophy syndrome Isolated bone marrow mastocytosis Epidermolysis bullosa simplex, generalized intermediate Linear nevus sebaceus syndrome Piebald trait-neurologic defects syndrome LUMBAR syndrome GAPO syndrome Bullous pemphigoid Trichorhinophalangeal syndrome Keratosis follicularis spinulosa decalvans Absence of fingerprints-congenital milia syndrome Ehlers-Danlos syndrome, spondylocheirodysplastic type Syringocystadenoma papilliferum Syndromic oculocutaneous albinism Pemphigus vulgaris Orofaciodigital syndrome type 1 Junctional epidermolysis bullosa-pyloric atresia syndrome Nail-patella syndrome PTEN hamartoma tumor syndrome Sebocystomatosis Aplasia cutis congenita Minimal pigment oculocutaneous albinism type 1 Exfoliative ichthyosis Trichodysplasia-amelogenesis imperfecta syndrome ADULT syndrome Junctional epidermolysis bullosa, generalized intermediate Localized junctional epidermolysis bullosa, non-Herlitz type Haim-Munk syndrome Porokeratotic eccrine ostial and dermal duct nevus Dermoodontodysplasia Temperature-sensitive oculocutaneous albinism type 1 Recessive aplasia cutis congenita of limbs Junctional epidermolysis bullosa inversa Xeroderma pigmentosum-Cockayne syndrome complex Sparse hair-short stature-skin anomalies syndrome Congenital panfollicular nevus NEVADA syndrome Aplasia cutis congenita-intestinal lymphangiectasia syndrome Pili torti Sézary syndrome Genetic hypopigmentation of the skin Junctional epidermolysis bullosa, generalized severe Ehlers-Danlos syndrome type 2 Pili torti-onychodysplasia syndrome Ito hypomelanosis Aplasia cutis-myopia syndrome SCALP syndrome Neurocutaneous melanocytosis Familial isolated trichomegaly Oculocutaneous albinism type 1 Pili torti-developmental delay-neurological abnormalities syndrome Focal facial dermal dysplasia type I Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency Late-onset junctional epidermolysis bullosa Angioosteohypertrophic syndrome Monilethrix Pilodental dysplasia-refractive errors syndrome Marginal papular palmoplantar keratoderma Seborrhea-like dermatitis with psoriasiform elements Recessive dystrophic epidermolysis bullosa inversa Megalencephaly-capillary malformation-polymicrogyria syndrome Hereditary coproporphyria Acral self-healing collodion baby Severe generalized recessive dystrophic epidermolysis bullosa Acral peeling skin syndrome Primary cutaneous B-cell lymphoma Muckle-Wells syndrome Familial atypical multiple mole melanoma syndrome Meige disease Cockayne syndrome type 2 Dystrophic epidermolysis bullosa Transient bullous dermolysis of the newborn Waardenburg syndrome Chédiak-Higashi syndrome Pilomatrixoma Genetic dermis elastic tissue disorder Epidermolysis bullosa simplex Pretibial dystrophic epidermolysis bullosa Cockayne syndrome type 1 Loose anagen syndrome Disease with focal palmoplantar keratoderma as a major feature Lymphoadenopathic mastocytosis with eosinophilia Non-hereditary late-onset primary lymphedema Geroderma osteodysplastica Cutaneous neuroendocrine carcinoma Junctional epidermolysis bullosa Annular epidermolytic ichthyosis Ringed hair disease Mycosis fungoides and variants Congenital erythropoietic porphyria Hereditary painful callosities Pityriasis rubra pilaris Ectodermal dysplasia-blindness syndrome Genetic skin vascular disorder Acute intermittent porphyria Woolly hair Cockayne syndrome type 3 Focal facial dermal dysplasia type III Ehlers-Danlos syndrome with periventricular heterotopia Paraneoplastic pemphigus Oculocutaneous albinism type 7 Classic mast cell leukemia Progressive osseous heteroplasia Böök syndrome Hereditary poikiloderma Marie Unna hereditary hypotrichosis Hidrotic ectodermal dysplasia, Christianson-Fourie type Isolated congenital anonychia Woolly hair nevus Mandibular hypoplasia-deafness-progeroid syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Hidrotic ectodermal dysplasia, Halal type Autosomal erythropoietic protoporphyria Genetic subcutaneous tissue disorder Suprabasal epidermolysis bullosa simplex Genetic mixed dermis disorder Ehlers-Danlos syndrome type 7B Keratosis palmaris et plantaris-clinodactyly syndrome Tricho-retino-dento-digital syndrome Amelocerebrohypohidrotic syndrome Dowling-Degos disease Autosomal dominant hypohidrotic ectodermal dysplasia Ehlers-Danlos syndrome type 7A Generalized peeling skin syndrome Hypertrichosis cubiti Odontomicronychial dysplasia Onychocytic matricoma Pili bifurcati Acrokeratoelastoidosis of Costa Diffuse palmoplantar keratoderma-acrocyanosis syndrome Isolated congenital onychodysplasia Cartilage-hair hypoplasia Linear atrophoderma of Moulin Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome Familial reactive perforating collagenosis Autosomal dominant epidermolytic ichthyosis Anonychia congenita totalis Dermatopathia pigmentosa reticularis Basal epidermolysis bullosa simplex Hypertrichosis lanuginosa congenita Familial progressive hyperpigmentation Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Lamellar ichthyosis Rare nail tumor Dermochondrocorneal dystrophy Acroosteolysis-keloid-like lesions-premature aging syndrome Dyschromatosis symmetrica hereditaria Hereditary palmoplantar keratoderma, Gamborg-Nielsen type Primary lymphedema Muir-Torre syndrome AREDYLD syndrome Aleukemic mast cell leukemia Erythrokeratoderma ''en cocardes'' Hereditary acrokeratotic poikiloderma, Weary type Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Epidermolysis bullosa simplex due to plakophilin deficiency Acrokeratosis verruciformis of Hopf Progressive symmetric erythrokeratodermia Albinism-deafness syndrome Focal facial dermal dysplasia Kindler syndrome Linear and whorled nevoid hypermelanosis Hair defect-photosensitivity-intellectual disability syndrome Erythrokeratodermia variabilis Chondroectodermal dysplasia with night blindness Lacrimoauriculodentodigital syndrome Congenital lethal erythroderma X-linked hypohidrotic ectodermal dysplasia Acquired ichthyosis Rothmund-Thomson syndrome Bathing suit ichthyosis Acrogeria Hermansky-Pudlak syndrome with pulmonary fibrosis Ectodermal dysplasia, trichoodontoonychial type Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome Reticulate acropigmentation of Kitamura Wiedemann-Rautenstrauch syndrome Idiopathic trachyonychia Focal acral hyperkeratosis Spinocerebellar ataxia type 34 Trichofolliculoma Hypodontia-dysplasia of nails syndrome Superficial epidermolytic ichthyosis Onychomatricoma Lelis syndrome Diffuse lymphatic malformation Uncombable hair syndrome Focal dermal hypoplasia Disseminated superficial actinic porokeratosis Genetic photodermatosis Erythromelalgia Lipedema Disease with punctate palmoplantar keratoderma as a major feature Steatocystoma multiplex-natal teeth syndrome Acral dystrophic epidermolysis bullosa Harlequin ichthyosis Ehlers-Danlos syndrome Scalp defects-postaxial polydactyly syndrome Familial multiple trichoepithelioma Hermansky-Pudlak syndrome Gorlin-Chaudhry-Moss syndrome Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Xeroderma pigmentosum variant Multiple benign circumferential skin creases on limbs Alopecia-contractures-dwarfism-intellectual disability syndrome Primary cutaneous T-cell lymphoma Alopecia antibody deficiency Osteopathia striata-pigmentary dermopathy-white forelock syndrome Oculocutaneous albinism type 2 Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Recessive X-linked ichthyosis Oculocutaneous albinism type 1A Hidrotic ectodermal dysplasia Focal facial dermal dysplasia type II Porokeratosis of Mibelli Nevus of Ota Rothmund-Thomson syndrome type 1 Alopecia-epilepsy-pyorrhea-intellectual disability syndrome CLOVES syndrome Oculocutaneous albinism type 4 Familial normophosphatemic tumoral calcinosis Oculocutaneous albinism type 3 Generalized basaloid follicular hamartoma syndrome Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Cockayne syndrome Incontinentia pigmenti Oculocutaneous albinism Porokeratosis plantaris palmaris et disseminata Oculocutaneous albinism type 1B Dominant dystrophic epidermolysis bullosa, nails only Autosomal dominant palmoplantar keratoderma and congenital alopecia Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Autosomal dominant cutis laxa Skin fragility-woolly hair-palmoplantar keratoderma syndrome Epidermolysis bullosa simplex with circinate migratory erythema Cutis marmorata telangiectatica congenita Porphyria Oculocutaneous albinism type 5 Juvenile xanthogranuloma Corneodermatoosseous syndrome Autosomal recessive cutis laxa type 2 Hutchinson-Gilford progeria syndrome Focal facial dermal dysplasia type IV Autosomal recessive cutis laxa type 1 Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Hypohidrotic ectodermal dysplasia Hermansky-Pudlak syndrome without pulmonary fibrosis Congenital smooth muscle hamartoma Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome Farber disease RIN2 syndrome Rothmund-Thomson syndrome type 2 Occipital horn syndrome Trichorhinophalangeal syndrome type 1 and 3 Proteus syndrome Hallermann-Streiff syndrome Brittle cornea syndrome Dahlberg-Borer-Newcomer syndrome Erythrokeratoderma variabilis progressiva Nevus of Ito Epidermolysis bullosa simplex with pyloric atresia Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering Isolated congenital digital clubbing CHIME syndrome Cowden syndrome Hypohidrotic ectodermal dysplasia with immunodeficiency Familial multiple fibrofolliculoma Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature ALDH18A1-related De Barsy syndrome Crandall syndrome Toriello-Lacassie-Droste syndrome Cronkhite-Canada syndrome Lethal acantholytic epidermolysis bullosa Ehlers-Danlos syndrome due to tenascin-X deficiency Cleft lip/palate-ectodermal dysplasia syndrome Familial progressive hyper- and hypopigmentation Odonto-tricho-ungual-digito-palmar syndrome Leukoencephalopathy-palmoplantar keratoderma syndrome Striate palmoplantar keratoderma KID syndrome Pachydermoperiostosis Congenital generalized hypertrichosis, Ambras type Keratolytic winter erythema Leukonychia totalis Arterial tortuosity syndrome Pure hair and nail ectodermal dysplasia Non-hereditary congenital primary lymphedema Choroidal atrophy-alopecia syndrome Schöpf-Schulz-Passarge syndrome Ectodermal dysplasia with natal teeth, Turnpenny type Hartnup disease Frontonasal dysplasia with alopecia and genital anomaly Ehlers-Danlos syndrome, vascular-like type Ehlers-Danlos syndrome, progeroid type Oculocutaneous albinism type 6 CEDNIK syndrome Milroy disease X-linked reticulate pigmentary disorder Curly hair-acral keratoderma-caries syndrome Limb-mammary syndrome Hereditary acrokeratotic poikiloderma of Kindler-Weary Familial melanoma Hypotrichosis with juvenile macular degeneration Cutis laxa Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Epidermal nevus syndrome UV-sensitive syndrome Generalized pustular psoriasis Ameloonychohypohidrotic syndrome Atrichia with papular lesions X-linked Ehlers-Danlos syndrome Hermansky-Pudlak syndrome type 7 Naegeli-Franceschetti-Jadassohn syndrome Familial cylindromatosis Diffuse cutaneous mastocytosis Ehlers-Danlos syndrome, fibronectinemic type Mal de Meleda Waardenburg syndrome type 1 Palmoplantar keratoderma, Nagashima type Pseudoxanthoma elasticum Cutaneous mastocytoma Waardenburg syndrome type 2 Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Oley syndrome Deaf blind hypopigmentation syndrome, Yemenite type Encephalocraniocutaneous lipomatosis Trichodental syndrome Waardenburg syndrome type 3 Hypotrichosis simplex of the scalp Familial multiple nevi flammei Autosomal dominant diffuse mutilating palmoplantar keratoderma Maculopapular cutaneous mastocytosis Buschke-Ollendorff syndrome Tricho-dento-osseous syndrome Multiple symmetric lipomatosis Trichodermodysplasia-dental alterations syndrome Ehlers-Danlos syndrome, cardiac valvular type Follicular atrophoderma-basal cell carcinoma Large congenital melanocytic nevus Kein Name gefunden Hypopigmentation-punctate palmoplantar keratoderma syndrome Trichoodontoonychial dysplasia Darier disease Hereditary sclerosing poikiloderma, Weary type Proliferating trichilemmal cyst Cerebellar ataxia-ectodermal dysplasia syndrome Craniofaciofrontodigital syndrome Deafness-enamel hypoplasia-nail defects syndrome Congenital reticular ichthyosiform erythroderma Hemihyperplasia-multiple lipomatosis syndrome Autosomal dominant trichoodontoonychodysplasia-syndactyly Werner syndrome Ehlers-Danlos/osteogenesis imperfecta syndrome Familial keratoacanthoma Fanconi anemia Parana hard skin syndrome Hermansky-Pudlak syndrome type 8 Dermatomyositis Trichothiodystrophy Neurofibromatosis type 3 Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome Transgrediens et progrediens palmoplantar keratoderma Cutaneous mastocytosis Verrucous nevus Carvajal syndrome Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Inflammatory linear verrucous epidermal nevus Trichodysplasia-xeroderma syndrome Blepharo-cheilo-odontic syndrome LOC syndrome Netherton syndrome Ehlers-Danlos syndrome, musculocontractural type Keratosis pilaris atrophicans Acanthokeratolytic verrucous nevus Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Neurofibromatosis type 1 Ichthyosis follicularis-alopecia-photophobia syndrome Erythropoietic uroporphyria associated with myeloid malignancy Mastocytosis Poikiloderma with neutropenia Neurofibromatosis type 2 Xeroderma pigmentosum Epidermolysis bullosa simplex superficialis Porphyria variegata Autosomal recessive nail dysplasia Trichorhinophalangeal syndrome type 2 Epidermolysis bullosa simplex, autosomal recessive K14 Acute hepatic porphyria Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Deafness-onychodystrophy syndrome Bullous dystrophy, macular type Centripetalis recessive dystrophic epidermolysis bullosa Progeria-short stature-pigmented nevi syndrome Rare systemic or rheumatologic disease Junctional epidermolysis bullosa, non-Herlitz type Atypical Werner syndrome Graham Little-Piccardi-Lassueur syndrome Hepatoerythropoietic porphyria Bullous diffuse cutaneous mastocytosis Griscelli disease type 2 Rare lymphatic malformation Telangiectasia macularis eruptiva perstans Dystrophic epidermolysis bullosa pruriginosa Chronic hepatic porphyria Hermansky-Pudlak syndrome with neutropenia Griscelli disease type 1 De Barsy syndrome Familial anetoderma Recessive dystrophic epidermolysis bullosa, generalized intermediate Pemphigus vegetans Dubowitz syndrome Progeroid syndrome, Petty type Maffucci syndrome Conductive deafness-ptosis-skeletal anomalies syndrome Griscelli disease type 3 Familial primary localized cutaneous amyloidosis Anonychia-onychodystrophy syndrome Ataxia-telangiectasia Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease Pemphigus foliaceus Diffuse palmoplantar keratoderma with painful fissures Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature Mast cell sarcoma Microphthalmia with linear skin defects syndrome Pemphigus erythematosus Hermansky-Pudlak syndrome type 9 COFS syndrome Indolent systemic mastocytosis Mast cell leukemia Ehlers-Danlos syndrome, periodontitis type Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Hypotrichosis-deafness syndrome Phakomatosis cesiomarmorata Aggressive systemic mastocytosis PENS syndrome Granulomatous slack skin Severe dermatitis-multiple allergies-metabolic wasting syndrome Extracutaneous mastocytoma Phakomatosis cesioflammea Gorlin syndrome Familial cutaneous collagenoma Blue rubber bleb nevus Neonatal inflammatory skin and bowel disease Dyschromatosis universalis hereditaria Proteus-like syndrome Pseudoxanthomatous diffuse cutaneous mastocytosis Stiff skin syndrome Fried's tooth and nail syndrome Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome Nevus comedonicus syndrome Cystic hygroma Pyramidal molars-abnormal upper lip syndrome Phakomatosis spilorosea Becker nevus syndrome Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome Griscelli disease Hyperkeratosis-hyperpigmentation syndrome Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Bannayan-Riley-Ruvalcaba syndrome Pellagra-like skin rash-neurological manifestations syndrome Ichthyosis Rombo syndrome Microcystic lymphatic malformation Palpebral sebaceous gland tumor Noonan syndrome-like disorder with loose anagen hair Ectodermal dysplasia-sensorineural deafness syndrome Autosomal ichthyosis syndrome Macrocystic lymphatic malformation SAPHO syndrome Pili gemini Terminal osseous dysplasia-pigmentary defects syndrome Palmoplantar keratoderma-sclerodactyly syndrome Tietz syndrome Autosomal recessive hypohidrotic ectodermal dysplasia X-linked ichthyosis syndrome Anonychia with flexural pigmentation Cardiofaciocutaneous syndrome Superficial pemphigus Familial articular hypermobility syndrome Pyogenic arthritis-pyoderma gangrenosum-acne syndrome Bazex-Dupré-Christol syndrome Familial benign chronic pemphigus Acquired epidermolysis bullosa Generalized dominant dystrophic epidermolysis bullosa Familial tumoral calcinosis Mucous membrane pemphigoid Isolated anterior cervical hypertrichosis Hereditary leiomyomatosis and renal cell cancer Linear IgA dermatosis Focal palmoplantar keratoderma with joint keratoses Brooke-Spiegler syndrome Hereditary palmoplantar keratoderma Autosomal ichthyosis syndrome with prominent hair abnormalities Other genetic epidermal disease Schinzel-Giedion syndrome Zlotogora-Ogur syndrome X-linked congenital generalized hypertrichosis Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome Gingival fibromatosis-hypertrichosis syndrome Herpetiform pemphigus Autosomal dominant deafness-onychodystrophy syndrome Juvenile hyaline fibromatosis Inherited epidermolysis bullosa Naxos disease Oculodentodigital dysplasia Genetic epidermal disorder Autosomal recessive cutis laxa type 2A Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Roch-Leri mesosomatous lipomatosis Alopecia Contractures-ectodermal dysplasia-cleft lip/palate syndrome Punctate palmoplantar keratoderma type 1 Inherited non-syndromic ichthyosis Fibrosarcoma Legius syndrome Epidermolysis bullosa simplex with muscular dystrophy Lipoid proteinosis Undifferentiated connective tissue syndrome X-linked dominant chondrodysplasia punctata DOORS syndrome Oculoosteocutaneous syndrome Isolated hair shaft abnormality Birt-Hogg-Dubé syndrome Erythema palmare hereditarium Ledderhose disease Ichthyosis hystrix of Curth-Macklin Diffuse cutaneous systemic sclerosis Ehlers-Danlos syndrome, kyphoscoliotic and deafness type Alopecia-intellectual disability syndrome Hypertrichosis Antecubital pterygium syndrome EEC syndrome Björnstad syndrome Tuberous sclerosis complex Cooks syndrome Dermotrichic syndrome Inherited ichthyosis syndromic form Pustulosis palmaris et plantaris PYCR1-related De Barsy syndrome Punctate palmoplantar keratoderma type 2 EEM syndrome H syndrome Isolated nail anomaly Superficial fibromatosis Chilblain lupus Autosomal recessive cutis laxa type 2B Syndromic hair shaft abnormality Bloom syndrome Ichthyosis hystrix gravior Primary cutis verticis gyrata Rare cutaneous lupus erythematosus Autosomal recessive multiple pterygium syndrome Familial cold urticaria Ehlers-Danlos syndrome, arthrochalasis type Porphyria cutanea tarda Oculotrichodysplasia Hypertrophic or verrucous lupus erythematosus Scalp-ear-nipple syndrome Pachyonychia congenita Autosomal recessive congenital ichthyosis Pemphigoid gestationis Acrodermatitis continua of Hallopeau Ehlers-Danlos syndrome, kyphoscoliotic type Discoid lupus erythematosus Isolated diffuse palmoplantar keratoderma Oculocerebral hypopigmentation syndrome, Cross type Punctate palmoplantar keratoderma Inherited ichthyosis Syndromic nail anomaly Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome Ehlers-Danlos syndrome, dermatosparaxis type Syndromic recessive X-linked ichthyosis Atrophoderma vermiculata Ectodermal dysplasia syndrome Diffuse palmoplantar keratoderma Limited cutaneous systemic sclerosis Lupus erythematosus tumidus Vici syndrome Odonto-onycho-dermal dysplasia Genetic acrokeratoderma CLAPO syndrome Subacute cutaneous lupus erythematosus Lymphedema-distichiasis syndrome Calcifying aponeurotic fibroma Odonto-onycho dysplasia-alopecia syndrome Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Genetic erythrokeratoderma Familial generalized lentiginosis Lupus erythematosus panniculitis Porphyria due to ALA dehydratase deficiency Adult T-cell leukemia/lymphoma Odontotrichomelic syndrome Carney complex Primary cutaneous CD30+ T-cell lymphoproliferative disease

Provided care options 10

# Contact person
1
Spezialsprechstunde für Autoinflammationserkrankungen und Akne inversa
Prof. Dr. med. Kathrin Giehl, Dr. med. Daniela Hartmann

089 440056391
Email
Website
Sprechzeiten: Donnerstag Nachmittag nach Vereinbarung
This consultation offers genetic counselling.

2
Spezialsprechstunde für bullöse Autoimmunkrankheiten
Dr. med. Tanja von Braunmühl

089 440056391
Email
Website
Sprechzeiten: Mi 14:00 - 16.00 Uhr nach Vereinbarung.

3
Spezialsprechstunde für das Birt-Hogg-Dubé Syndrom
Dr. med. Elke Sattler, Prof. Dr. med. Ortrud Steinlein

089 440056391
Email
Website
Sprechzeiten nach Vereinbarung.
This consultation offers genetic counselling.

4
Spezialsprechstunde für Genodermatosen
Prof. Dr. med. Kathrin Giehl, Prof. Dr. med. Heinrich Schmidt

089 440056391
Email
Website
Sprechzeiten nach Vereinbarung.
This consultation offers genetic counselling.

5
Spezialsprechstunde für Kollagenosen
Dr. Dr. med. Miklos Sardy, Prof. Dr. med. Peter Thomas, Dr. med. Orsolya Horváth

089 440056391
Email
Website
Sprechzeiten: Di 13:30 - 15:30 Uhr nach Vereinbarung.

6
Spezialsprechstunde für Mastozytosen
Prof. Dr. med. Franziska Rueff

089 440056391
Email
Website
Sprechzeiten nach Vereinbarung.

7
Spezialsprechstunde für pädiatrische Dermatologie
Prof. Dr. med. Kathrin Giehl, Prof. Dr. med. Heinrich Schmidt

089 440056391
Email
Website
Sprechzeiten nach Vereinbarung.
This consultation offers genetic counselling.

8
Spezialsprechstunde für seltene Haarekrankungen
Prof. Dr. med. Hans Wolff

089 440056391
Email
Website
Sprechzeiten nach Vereinbarung.
This consultation offers genetic counselling.

9
Spezialsprechstunde für seltene Hauttumoren
Prof. Dr. med. Hans Wolff, Dr. med. Kathrin Giehl

089 440056391
Email
Website
Sprechzeiten nach Vereinbarung.

10
Spezialsprechstunde kutane Lymphome
Dr. med. Michael Flaig, Dr. med. Katharina Kilian

0049 89440056391
Email
Website
Sprechzeiten: Di 14:00 Uhr nach Vereinbarung.

11.56376514047546448.12910573370476Interdisziplinäres Zentrum für seltene und genetische Hautkrankheiten am LMU Klinikum München
Last updated: 09.07.2020