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Mapping of Health Care Providers
for People with Rare Diseases

Craniofaciales Centrum Würzburg (CFCW) am Universitätsklinikum Würzburg

Description of facility

Director / Spokesperson
Prof. Dr. med. Tilmann Schweitzer
Information
Care facility for adults and children
Description
Das Craniofaciale Centrum Würzburg betreut Patienten mit allen Formen von Fehlbildungen im Schädel- und Gesichtsbereich, insbesondere Patienten mit vorzeitigem Verschluss einer oder mehrerer Schädelnähte. Ein besonderer Schwerpunkt liegt dabei im Bereich der syndromalen Erkrankungen. Das Zentrum arbeitet interdisziplinär und multiprofessionell, führt Studien durch und ist an nationalen sowie internationalen Forschungsprojekten beteiligt.

Beteiligte Einrichtungen:
Klinik und Poliklinik für Neurochirurgie, Sektion für pädiatrische Neurochirurgie
Klinik und Poliklinik für Mund-, Kiefer- und Plastische Gesichtschirurgie
Poliklinik für Kieferorthopädie
Kinderklinik und Poliklinik
Klinik und Poliklinik für Hals-, Nasen- und Ohrenkrankheiten, plastische und ästhetische Operationen
Augenklinik und Poliklinik
Institut für Humangenetik der Universität Würzburg

Consultation hours

nach Vereinbarung.

Care provisions

This facility offers the following
  • Social / legal advice
  • Genetic counselling
  • Clinical studies / research
  • Diagnostic
  • Therapy

Contact

Craniofaciale Sprechstunde
0931 20174862
Website https://www.ukw.de/behandlungszentren/craniofaciales-centrum-wuerzburg/startseite/

Secondary Contact

Erstvorstellung
0931 20124840
glanderkoe_m@ukw.de

Address

Pleicherwall 2
97070 Würzburg

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Languages

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

Preview of the assigned diseases 10

Goldenhar syndrome Pfeiffer syndrome type 1 Pfeiffer syndrome type 3 Pfeiffer syndrome type 2 Crouzon syndrome-acanthosis nigricans syndrome Rare otorhinolaryngologic disease Nager syndrome Isolated encephalocele Autosomal dominant otospondylomegaepiphyseal dysplasia Osteosclerosis-developmental delay-craniosynostosis syndrome Atelosteogenesis type II Saethre-Chotzen syndrome Atelosteogenesis type III Cloverleaf skull-multiple congenital anomalies syndrome Frontonasal dysplasia Holoprosencephaly-craniosynostosis syndrome Isotretinoin syndrome Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome Dobrow syndrome Acrocephalosyndactyly Familial lambdoid synostosis Non-syndromic craniosynostosis Fetal valproate spectrum disorder SCARF syndrome Baller-Gerold syndrome Rare maxillo-facial surgical disease Aminopterin/methotrexate embryofetopathy Syndromic craniosynostosis Indomethacin embryofetopathy Smith-Lemli-Opitz syndrome Intellectual disability-brachydactyly-Pierre Robin syndrome Fetal iodine syndrome Smith-Magenis syndrome Cocaine embryofetopathy Fetal hydantoin syndrome Kabuki syndrome Fetal trimethadione syndrome Vitamin K antagonist embryofetopathy Fetal alcohol syndrome Lethal occipital encephalocele-skeletal dysplasia syndrome Shprintzen-Goldberg syndrome Fetal methylmercury syndrome Cardiocranial syndrome, Pfeiffer type Fetal minoxidil syndrome Phenobarbital embryopathy Stickler syndrome Toluene embryopathy Methimazole embryofetopathy Cranioectodermal dysplasia Pierre Robin syndrome associated with collagen disease Non-syndromic bilambdoid and sagittal craniosynostosis Diabetic embryopathy Cantú syndrome Pierre Robin syndrome associated with a chromosomal anomaly Teebi-Shaltout syndrome Frontofacionasal dysplasia Rare disease with Pierre Robin syndrome SPECC1L-related hypertelorism syndrome Isolated oxycephaly Carpenter syndrome Craniofrontonasal dysplasia Autosomal recessive Stickler syndrome Craniofrontonasal dysplasia-Poland anomaly syndrome Oculomaxillofacial dysostosis 22q11.2 deletion syndrome TARP syndrome Fetal parvovirus syndrome Craniomicromelic syndrome Pierre Robin syndrome associated with branchial archs anomalies Isolated cloverleaf skull syndrome Oculoauriculofrontonasal syndrome Pierre Robin syndrome associated with bone disease Dysostosis with predominant craniofacial involvement Craniosynostosis, Philadelphia type Maternal phenylketonuria Craniotelencephalic dysplasia Pfeiffer syndrome Frontorhiny Teratogenic Pierre Robin syndrome Craniosynostosis-cataract syndrome Waardenburg syndrome Craniosynostosis Pseudoaminopterin syndrome Craniosynostosis-fibular aplasia syndrome Maternal hyperthermia-induced birth defects X-linked intellectual disability-plagiocephaly syndrome Craniosynostosis-dysmorphism-brachydactyly syndrome Isolated Pierre Robin syndrome Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome Familial scaphocephaly syndrome Jackson-Weiss syndrome Craniosynostosis, Boston type Non-syndromic sagittal craniosynostosis Familial osteodysplasia, Anderson type Craniosynostosis-dental anomalies Familial scaphocephaly syndrome, McGillivray type Treacher-Collins syndrome Isolated plagiocephaly Non-syndromic bicoronal craniosynostosis Cloverleaf skull-asphyxiating thoracic dysplasia syndrome Curry-Jones syndrome Acromelic frontonasal dysplasia Rare sucking/swallowing disorder Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Goodman syndrome Cornelia de Lange syndrome Frontonasal dysplasia-alopecia-genital anomalies syndrome Crouzon syndrome Summitt syndrome Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome Craniolenticulosutural dysplasia Kniest dysplasia Muenke syndrome C syndrome Antley-Bixler syndrome Pai syndrome Apert syndrome Rare neoplastic disease Craniosynostosis-intracranial calcifications syndrome Stickler syndrome type 2 Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome Craniofaciofrontodigital syndrome Fragile X syndrome Stickler syndrome type 1 Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Lowry-MacLean syndrome Nasal encephalocele Trigonocephaly-broad thumbs syndrome Craniosynostosis-anal anomalies-porokeratosis syndrome Non-syndromic metopic craniosynostosis Oculoauriculovertebral spectrum with radial defects Hunter-McAlpine syndrome Trigonocephaly-short stature-developmental delay syndrome Acrocephalopolydactyly Atelosteogenesis type I Craniosynostosis, Herrmann-Opitz type Multiple synostoses syndrome
9.927240649.7986738Craniofaciales Centrum Würzburg (CFCW) am Universitätsklinikum Würzburg
Last updated: 17.07.2024