Craniofaciales Centrum Münster Assigned diseases:
In the following you will find the diseases that are treated in this facility:
Acalvaria
Adducted thumbs-arthrogryposis syndrome, Christian type
Ankyloblepharon filiforme adnatum-imperforate anus syndrome
Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
Arthrogryposis multiplex congenita-whistling face syndrome
Autosomal dominant popliteal pterygium syndrome
BOR syndrome
Beckwith-Wiedemann syndrome
CHARGE syndrome
Cantú syndrome
Cleft palate
Cleidocranial dysplasia
Cranial malformation
Craniodiaphyseal dysplasia
Craniofaciofrontodigital syndrome
Craniosynostosis
Delayed membranous cranial ossification
Dobrow syndrome
Dysostosis with predominant craniofacial involvement
EEC syndrome
Enlarged parietal foramina
Facial cleft
Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome
Familial osteodysplasia, Anderson type
Frontonasal dysplasia
Goldenhar syndrome
Hypoglossia/aglossia
Hypomandibular faciocranial dysostosis
Isolated Pierre Robin syndrome
Isolated ankyloblepharon filiforme adnatum
Isolated congenital syngnathia
Macroglossia
Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome
Marden-Walker syndrome
Maxillonasal dysplasia
Monosomy 18q
Morgagni-Stewart-Morel syndrome
Multiple pterygium-malignant hyperthermia syndrome
Non-syndromic bilambdoid and sagittal craniosynostosis
Oculoauriculovertebral spectrum with radial defects
Oculomaxillofacial dysostosis
Orofacial clefting syndrome
Orofaciodigital syndrome
Otomandibular dysplasia
Otopalatodigital syndrome
Popliteal pterygium syndrome
Postaxial acrofacial dysostosis
Proteus syndrome
Rare disease with Pierre Robin syndrome
Rare maxillo-facial surgical disease
Simpson-Golabi-Behmel syndrome
Simpson-Golabi-Behmel syndrome type 2
Syndrome or malformation associated with head and neck malformations
Teebi-Shaltout syndrome
Treacher-Collins syndrome
Van den Ende-Gupta syndrome
Van der Woude syndrome