SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik für Dermatologie, Venerologie und Allergologie an der Charité Berlin

Description of facility

Director / Spokesperson
Prof. Dr. med. Kamran Ghoreschi
Information
Care facility for adults and children
Description

Im Rahmen der Kinderdermatologischen Sprechstunde findet die Betreuung von Kindern zur Diagnostik von Hautveränderungen und Entwicklung von Therapiekonzepten statt.

Schwerpunktmäßig kümmert sich die Klinik um Kinder mit erblichen oder seltenen Hautkrankheiten, Autoimmunerkrankungen, Hautveränderungen im Rahmen von Syndromen, Nachsorge von hämato-onkologischen Patienten sowie die Betreuung von Kindern mit Haarerkrankungen.

Care provisions

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

Contact

Prof. Dr. med. Kamran Ghoreschi
030 450518062
030 450518911
Website https://derma.charite.de/

Address

Luisenstraße 2
10117 Berlin
Campus Charité Mitte

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Languages

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

Mentioned by the following facilities 1

Preview of the assigned diseases 4

Katarakt-Hypertrichose-Intelligenzminderung-Syndrom Syndrom des akromegaloiden Gesichtes mit Hypertrichose Tricho-rhino-phalangeales Syndrom Epidermolysis bullosa simplex durch Exophilin 5-Mangel Katarakt, kongenitale - Ichthyose Erythrodermie, ichthyosiforme kongenitale Marshall-Syndrom Dysplasie, kranioektodermale Epidermolysis bullosa simplex, generalisierte schwere ANE-Syndrom Ellis Van Creveld-Syndrom Keratoderma hereditarium mutilans mit Ichthyose Trichomegalie, isolierte, familiäre Form Teebi-Shaltout-Syndrom Alopecia totalis Epidermolysis bullosa simplex mit gesprenkelter Pigmentierung Epidermolysis bullosa simplex, lokalisierte Alopecia universalis Dermato-Osteolyse, kirgisischer Typ Selbstheilendes Kollodiumbaby, akrales Epidermolysis bullosa simplex, generalisierte intermediäre, autosomal-dominante Trichodysplasie - Amelogenesis imperfecta GAPO-Syndrom Epidermolysis bullosa, junktionale, generalisierte intermediäre Ichthyose-Hypotrichose-Syndrom PLEC-assoziierte intermediäre Epidermolysis bullosa simplex ohne extrakutane Beteiligung Oro-fazio-digitales Syndrom Typ 1 Epidermolysis bullosa, junktionale lokalisierte Epidermolysis bullosa, junctionale, generalisierte schwere Dermoodontodysplasie ADULT-Syndrom Selbstheilendes Kollodium-Baby Schütteres Haar - Kleinwuchs - Hautveränderungen Junktionale Epidermolysis bullosa mit Pylorusatresie Pili torti Epidermolysis bullosa, junktionale, spät beginnende Pili torti-Onychodysplasie-Syndrom Hypomelanose Typ Ito Epidermolysis bullosa inversa, junktionale Pili torti - Entwicklungsverzögerung - neurologische Anomalien Dysplasie, dermale faziale fokale, Typ I Monilethrix Dysplasie, pilo-dentale - Refraktionsanomalien Epidermolysis bullosa inversa, dystrophe, rezessive Peeling-Skin-Syndrom, lokalisiertes Epidermolysis bullosa, dystrophe, generalisierte schwere, autosomal-rezessive Epidermolysis bullosa, dystrophe Epidermolysis bullosa, dystrophe, selbstheilende Form Epidermolysis bullosa, dystrophe lokalisierte, prätibiale Form Epidermolysis bullosa simplex Lose Anagenhaar-Syndrom Ichthyose, exfoliative Epidermolysis bullosa, junktionale Ringelhaare Dysplasie, ektodermale - Blindheit Wollhaare Dysplasie, dermale faziale fokale, Typ III Fokale faziale dermale Dysplasie Book-Syndrom Hypotrichose, hereditäre kongenitale, Typ Marie Unna Dysplasie, ektodermale hidrotische, Typ Christianson-Fourie Wollhaarnaevus Osteosklerose - Ichthyose - vorzeitige Ovarialinsuffizienz Dysplasie, ektodermale hidrotische, Typ Halal Tricho-retino-dento-digitales Syndrom Peeling-Skin-Syndrom, generalisiertes Amelo-zerebro-hypohidrotisches Syndrom Dysplasie, ektodermale hypohidrotische, autosomal-dominante Hypertrichosis cubiti Pili bifurcati Hypertrichosis lanuginosa, erworbene Knorpel-Haar-Hypoplasie Ektodermale Dysplasie-Intelligenzminderung-ZNS-Fehlbildungen-Syndrom Ichthyose, epidermolytische, autosomal-dominante Epidermolysis bullosa simplex, basale Kongenitale Ichthyose-Intelligenzminderung-spastische Tetraplegie-Syndrom Hypertrichosis lanuginosa, kongenitale Peeling-Skin-Syndrom Typ A Dermatopathia pigmentosa reticularis Ichthyose, lamelläre Epidermolysis bullosa simplex, suprabasale Ichthyose, anuläre epidermolytische AREDYLD-Syndrom Leukomelanodermie-Infantilismus-Intelligenzminderung-Hypodontie-Hypotrichose-Syndrom Ektodermale Dysplasie-Hautfragilität-Syndrom Peeling-Skin-Syndrom Typ B Fokale faziale dermale Dysplasie Typ II Kindler Epidermolysis bullosa Lakrimo-aurikulo-dento-digitales Syndrom Erythrokeratodermia variabilis Haaranomalien - Photosensibilität - Intelligenzminderung Dysplasie, ektodermale hypohidrotische, X-chromosomale Dysplasie, ektodermale, tricho-odonto-onychaler Typ Wollhaare-Hypotrichose-evertierte Unterlippe-abstehende Ohren-Syndrom Hypodontie - Nageldysplasie Hypoplasie, fokale dermale Lelis-Syndrom Syndrom der nicht kämmbaren Haare Peeling-Skin-Syndrom, generalisiertes, Typ C Epidermolysis bullosa, dystrophe lokalisierte, akrale Form Bathing-suit-Ichthyose Harlekin-Ichthyose Gorlin-Chaudhry-Moss-Syndrom Alopezie-Kontrakturen-Kleinwuchs-Intelligenzminderung-Syndrom Epidermolysis bullosa, dystrophe, dominante, nur Nägel Alopezie mit Antikörper-Mangel Ichthyose, X-chromosomal-rezessive Dysplasie, ektodermale hidrotische Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Incontinentia pigmenti Autosomal dominant palmoplantar keratoderma and congenital alopecia Epidermolysis bullosa simplex with circinate migratory erythema Corneodermatoosseous syndrome Hypohidrotic ectodermal dysplasia Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Trichorhinophalangeal syndrome type 1 Hallermann-Streiff syndrome Dahlberg-Borer-Newcomer syndrome Curly hair-acral keratoderma-caries syndrome Epidermolysis bullosa simplex with pyloric atresia CHIME syndrome Crandall syndrome Focal facial dermal dysplasia type IV Hypohidrotic ectodermal dysplasia with immunodeficiency Ectodermal dysplasia with natal teeth, Turnpenny type Frontonasal dysplasia-alopecia-genital anomalies syndrome Congenital generalized hypertrichosis, Ambras type Choroidal atrophy-alopecia syndrome Odonto-tricho-ungual-digito-palmar syndrome Limb-mammary syndrome Schöpf-Schulz-Passarge syndrome Pure hair and nail ectodermal dysplasia Hypotrichosis with juvenile macular degeneration Amelo-onycho-hypohidrotic syndrome CEDNIK syndrome Quinquaud folliculitis decalvans Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Naegeli-Franceschetti-Jadassohn syndrome Cleft lip/palate-ectodermal dysplasia syndrome Atrichia with papular lesions Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Trichodental syndrome Hypotrichosis simplex of the scalp Tricho-dento-osseous syndrome Trichodermodysplasia-dental alterations syndrome Tricho-oculo-dermo-vertebral syndrome Trichoodontoonychial dysplasia Cerebellar ataxia-ectodermal dysplasia syndrome Deafness-enamel hypoplasia-nail defects syndrome Autosomal dominant trichoodontoonychodysplasia-syndactyly Trichothiodystrophy Ichthyosis-cheek-eyebrow syndrome Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Trichodysplasia-xeroderma syndrome Blepharo-cheilo-odontic syndrome Laryngo-onycho-cutaneous syndrome Netherton syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Ichthyosis-oral and digital anomalies syndrome Ichthyosis follicularis-alopecia-photophobia syndrome Autosomal recessive generalized epidermolysis bullosa simplex Congenital reticular ichthyosiform erythroderma Trichorhinophalangeal syndrome type 2 Hypotrichosis-deafness syndrome Junctional epidermolysis bullosa, non-Herlitz type Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Deafness-onychodystrophy syndrome Epidermolysis bullosa simplex superficialis Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form Graham Little-Piccardi-Lassueur syndrome Dystrophic epidermolysis bullosa pruriginosa Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome Centripetalis recessive dystrophic epidermolysis bullosa Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Dubowitz syndrome Conductive deafness-ptosis-skeletal anomalies syndrome Ichthyosis-prematurity syndrome Pyramidal molars-abnormal upper lip syndrome Fried's tooth and nail syndrome Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Noonan syndrome-like disorder with loose anagen hair Ectodermal dysplasia-sensorineural deafness syndrome Pili gemini Autosomal recessive hypohidrotic ectodermal dysplasia Ichthyosis Anonychia with flexural pigmentation Cardiofaciocutaneous syndrome Autosomal dominant generalized dystrophic epidermolysis bullosa Lichen planopilaris Cleft lip/palate-ectodermal dysplasia syndrome Schinzel-Giedion syndrome Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome X-linked congenital generalized hypertrichosis Gingival fibromatosis-hypertrichosis syndrome Inherited epidermolysis bullosa Contractures-ectodermal dysplasia-cleft lip/palate syndrome Ichthyosis hystrix gravior Autosomal ichthyosis syndrome with prominent hair abnormalities EEM syndrome Syndromic hair shaft abnormality Ichthyosis hystrix of Curth-Macklin Oculotrichodysplasia Scalp-ear-nipple syndrome Rare disorder with hypertrichosis Syndromic recessive X-linked ichthyosis Isolated hair shaft abnormality Björnstad syndrome Autosomal dominant deafness-onychodystrophy syndrome Oculodentodigital dysplasia Alopecia Frontal fibrosing alopecia DOORS syndrome Chondroectodermal dysplasia with night blindness Epidermolysis bullosa simplex with muscular dystrophy Alopecia-intellectual disability syndrome Isolated anterior cervical hypertrichosis EEC syndrome Lethal acantholytic erosive disorder Inherited ichthyosis syndromic form Oculoosteocutaneous syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Toriello-Lacassie-Droste syndrome X-linked dominant chondrodysplasia punctata Dermotrichic syndrome Cronkhite-Canada syndrome Superficial epidermolytic ichthyosis Cooks syndrome KID syndrome Ectodermal dysplasia syndrome Pseudopelade of Brocq Odonto-onycho-dermal dysplasia Odonto-onycho dysplasia-alopecia syndrome Autosomal ichthyosis syndrome with prominent neurologic signs Odontotrichomelic syndrome MEDNIK syndrome Papillon-Lefèvre syndrome Hereditary hypotrichosis with recurrent skin vesicles Johanson-Blizzard syndrome Johnson neuroectodermal syndrome Acrofacial dysostosis, Weyers type Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome Sjögren-Larsson syndrome Autosomal recessive congenital ichthyosis Peeling skin syndrome EEC syndrome and related disorders Autosomal ichthyosis syndrome with other associated signs Genetic hair anomaly Dyskeratosis congenita Autosomal recessive palmoplantar keratoderma and congenital alopecia CHILD syndrome Epidermolysis bullosa simplex due to BP230 deficiency Taurodontia-absent teeth-sparse hair syndrome Barber-Say syndrome Keratinopathic ichthyosis Bartsocas-Papas syndrome Epidermolysis bullosa simplex with anodontia/hypodontia Autosomal ichthyosis syndrome with fatal disease course Hypotrichosis simplex Ectodermal dysplasia-hyperhidrosis-cutaneous syndactyly syndrome

Provided care options 4

# Contact person
1
Spezialambulanz für genetische Haarerkrankungen
Information

030 450518065
Email
Website
Sprechzeiten nach Vereinbarung.

2
Spezialambulanz für Ichthyosen
Prof. Dr. Ulrike Blume-Peytavi, Dr. Karola Stieler

030 450518065
Email
Website
Sprechzeiten nach Vereinbarung.

3
Spezialambulanz für Ektodermale Dysplasie
Information

030 450518065
Email
Website
Sprechzeiten nach Vereinbarung.

4
Spezialambulanz für Epidermolysis bullosa
Information

030 450518065
Email
Website
Sprechzeiten nach Vereinbarung.

13.37852060794830552.52719129639235Klinik für Dermatologie, Venerologie und Allergologie an der Charité Berlin
Last updated: 14.09.2023